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| Product | Description | |
|---|---|---|
| 1-(1H-Benzotriazol-1-yl)-1-octanone | 1-(1H-Benzotriazol-1-yl)-1-octanone is a useful intermediate, which is used in several types of reactions such as the prearation of N-acylpiperidines via acylation. Group: Biochemicals. Grades: Highly Purified. CAS No. 58068-80-7. Pack Sizes: 250mg, 1g. Molecular Formula: C14H19N3O. US Biological Life Sciences. |  Worldwide |
| 17-Amino-10-oxo-3,6,12,15-tetraoxa-9-azaheptadecanoic Acid | 17-Amino-10-oxo-3,6,12,15-tetraoxa-9-azaheptadecanoic Acid is used for preparation of glutamic acid-containing acylating reagents for selective acylation of amino group(s) in peptides or proteins. Group: Biochemicals. Grades: Highly Purified. CAS No. 1143516-05-5. Pack Sizes: 100mg, 250mg. Molecular Formula: C12H24N2O7, Molecular Weight: 308.33. US Biological Life Sciences. | Worldwide |
| 1-Acetyl-1H-1,2,3-triazolo[4,5-b]pyridine | Acylation Reagents. Alternative Names: Acetyltriazolopyridine. CAS No. 107866-54-6. Molecular formula: C7H6N4O. Mole weight: 162.15. Purity: 0.97. IUPACName: 1-(triazolo[4,5-b]pyridin-1-yl)ethanone. Canonical SMILES: CC(=O)N1C2=C(N=CC=C2)N=N1. Density: 1.48g/cm³. Catalog: ACM107866546. |  |
| (1R,3R,4R)-(-)-3,5-Dinitrobenzoate Menthol | (1S,3S,4S)-(-)-3,5-dinitrobenzoate Menthol is an intermediate in the synthesis of (±)-Neoisomenthol (N389960) which is a useful synthetic intermediate. It is used to prepare alkyl and aryl esters by chemoselective acylation of alkyl and aryl alcohols with carboxylic acid anhydrides in the presence of magnesium bis (trifluoro methyl sulfonyl) amide under solvent-free conditions. Group: Biochemicals. Grades: Highly Purified. CAS No. 1195710-85-0. Pack Sizes: 50mg, 100mg. Molecular Formula: C17H22N2O6. US Biological Life Sciences. | Worldwide |
| 2,2'-Bis(diphenylphosphino)-1,1'-binaphthyl | Phosphine Ligand Kit component. Useful ligand for palladium-catalyzed carbon-nitrogen bond formation. Useful ligand for rhodium-catalyzed C-C bond formation. Useful ligand for palladium-catalyzed intramolecular acylation of aryl bromides via C-H activation. Used in the preparation of Buchwald third generation precatalyst. Used in methoxy directed Rhodium migration. Used in Nickel catalyzed C-N cross-coupling reactions. Group: Organic phosphine compounds. Alternative Names: F0001-2326; DB-009478; AC1LCPMX; (S)-2,2'-BIS(DIPHENYLPHOSPHINO)-1,1'-BINAPHTHYL; AN-10356; SC-19338; (S)-(-)-2,2'-Bis(diphenylphosphino)-1,1'-binaphthalene, puriss.; PubChem8136; TL8005203; (S)-(-)-2,2 inverted exclamation mark -Bis(diphenylphosphino)-1,1 inverted exclamation mark -binaphthalene. CAS No. 98327-87-8. Molecular formula: C44H32P2. Mole weight: 622.688g/mol. IUPACName: [1-(2-diphenylphosphanylnaphthalen-1-yl)naphthalen-2-yl]-diphenylphosphane. Canonical SMILES: C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=C (C4=CC=CC=C4C=C3)C5=C (C=CC6=CC=CC=C65)P (C7=CC=CC=C7)C8=CC=CC=C8. ECNumber: 616-304-7. Catalog: ACM98327878. | |
| 2,2'-Oxybis(ethylamine) Dihydrochloride | 2,2'-Oxybis(ethylamine) Dihydrochloride can be used as reactant/reagent in polyboramines for hydrogen release: polymers containing Lewis pairs in their backbone. It can also be used in synthetic preparation and antitrypanosomal activity of adenosines via amination of chloropurinyl deoxyribofuranose with aminoethoxy ethylamine, followed by polymer-supported acylation of carboxylic acids. Group: Biochemicals. Grades: Highly Purified. CAS No. 60792-79-2. Pack Sizes: 250mg, 500mg. Molecular Formula: C4H12N2O 2HCl, Molecular Weight: 104.1523646. US Biological Life Sciences. | Worldwide |
| 2,5-Diacetoxytoluene | 2,5-Diacetoxytoluene can be used to investigate the kinetics of co-?polyesters of hydroquinone diacetate and its methyl derivative. It is also a useful reagent to prepare regioselective O-?acylation of polyphenols. Group: Biochemicals. Grades: Highly Purified. CAS No. 717-27-1. Pack Sizes: 5g, 10g. Molecular Formula: C11H12O4, Molecular Weight: 208.21. US Biological Life Sciences. | Worldwide |
| 2-Bromodibenzofuran | 2-Bromodibenzofuran is a brominated derivative of Dibenzofuran (D417185); a reagent in Friedel-Crafts acylation. Group: Biochemicals. Grades: Highly Purified. CAS No. 86-76-0. Pack Sizes: 250mg, 1g. Molecular Formula: C12H7BrO, Molecular Weight: 247.09. US Biological Life Sciences. | Worldwide |
| 3,4-Dichloroisocoumarin | 3,4-Dichloroisocoumarin is a potent serine-protease and SrLip inhibitor (K i for SrLip: 26.6 μM). 3,4-Dichloroisocoumarin is opened by serine proteases and then undergoes acylation with the enzyme, thereby inhibiting protease activity. 3,4-Dichloroisocoumarin can induce DNA fragmentation and Apoptosis. 3,4-Dichloroisocoumarin can be used in the research of multiple fields such as tumors, cardiovascular disease and enzyme catalytic mechanisms [1] [2] [3] [4] [5]. Uses: Scientific research. Group: Natural products. CAS No. 51050-59-0. Pack Sizes: 5 mg; 10 mg. Product ID: HY-126034. |  |
| 4-Chlorotoluene | 4-Chlorotoluene is used in a variety of organic synthesis, such as acting as coupling precursors for palladium-catalyzed acylation of acetanilides. Group: Biochemicals. Grades: Highly Purified. CAS No. 106-43-4. Pack Sizes: 10g, 50g, 100g. Molecular Formula: C?H?Cl. US Biological Life Sciences. | Worldwide |
| 4-Dimethylaminopyridine | A highly efficient catalyst for acylation reactions. Group: Biochemicals. Alternative Names: N,N-Dimethyl-4-pyridinamine. Grades: Highly Purified. CAS No. 1122-58-3. Pack Sizes: 25g. US Biological Life Sciences. | Worldwide |
| 4-Tert-Butylcalix[4]Arene | 4-Tert-Butylcalix[4]Arene. Uses: Starting material for further derivatization, including halogenation, acylation, and diazo coupling. Group: Macrocyclessupramolecular host materials. Alternative Names: P-TERT-BUTYLCALIX[4]ARENE; TETRA-TERT-BUTYL(TETRAHYDROXY)CALIX[4]ARENE; AKOS 43; 4-TERT-BUTYLCALIX[4]ARENE; 4-T-BUTYLCALIX[4]ARENE; ETHYL 2-([5, 11, 17, 23-TETRA(TERT-BUTYL)-26, 27, 28-TRIS(2-ETHOXY-2-OXYETHOXY)PENTACYCLO[19.3.1.1(3, 7).1(9, 13).1(15, 19)]OCTACOSA-1(2. CAS No. 60705-62-6. Pack Sizes: Packaging 5, 25 g in glass bottle. Product ID: 5, 11, 17, 23-tetratert-butylpentacyclo[19.3.1.13, 7.19, 13.115, 19]octacosa-1(24), 3, 5, 7(28), 9, 11, 13(27), 15(26), 16, 18, 21(25), 22-dodecaene-25, 26, 27, 28-tetrol. Molecular formula: 648.91. Mole weight: C44H56O4. CC (C) (C)C1=CC2=C (C (=C1)CC3=CC (=CC (=C3O)CC4=CC (=CC (=C4O)CC5=C (C (=CC (=C5)C (C) (C)C)C2)O)C (C) (C)C)C (C) (C)C)O. 1S/C44H56O4/c1-41 (2, 3)33-17-25-13-27-19-34 (42 (4, 5)6)21-29 (38 (27)46)15-31-23-36 (44 (10, 11)12)24-32 (40 (31)48)16-30-22-35 (43 (7, 8)9)20-28 (39 (30)47)14-26 (18-33)37 (25)45/h17-24, 45-48H, 13-16H2, 1-12H3. NVKLTRSBZLYZHK-UHFFFAOYSA-N. ≥ 97%. |  |
| 4-Tert-Butylcalix[4]Arene | Starting material for further derivatization, including halogenation, acylation, and diazo coupling. Group: Polymer/macromolecule. Alternative Names: P-TERT-BUTYLCALIX[4]ARENE;TETRA-TERT-BUTYL(TETRAHYDROXY)CALIX[4]ARENE;AKOS 43;4-TERT-BUTYLCALIX[4]ARENE;4-T-BUTYLCALIX[4]ARENE;ETHYL 2-([5, 11, 17, 23-TETRA(TERT-BUTYL)-26, 27, 28-TRIS(2-ETHOXY-2-OXYETHOXY)PENTACYCLO[19.3.1.1(3, 7).1(9, 13).1(15, 19)]OCTACOSA-1(2. CAS No. 60705-62-6. Molecular formula: C44H56O4. Mole weight: 648.91. Purity: ≥ 97%. IUPACName: 5, 11, 17, 23-tetratert-butylpentacyclo[19.3.1.13, 7.19, 13.115, 19]octacosa-1(24), 3, 5, 7(28), 9, 11, 13(27), 15(26), 16, 18, 21(25), 22-dodecaene-25, 26, 27, 28-tetrol. Canonical SMILES: CC (C) (C)C1=CC2=C (C (=C1)CC3=CC (=CC (=C3O)CC4=CC (=CC (=C4O)CC5=C (C (=CC (=C5)C (C) (C)C)C2)O)C (C) (C)C)C (C) (C)C)O. Catalog: ACM60705626-1. | |
| 5S rRNA modificator | 5S rRNA modificator is a suitable electrophile for 2'-hydroxyl acylation on structured RNA molecules, yielding accurate structural information comparable to that obtained with existing probes; 5S rRNA RNA modification. Synonyms: 5S rRNA modificator. Grades: >98%. CAS No. 1415238-77-5. Molecular formula: C9H8N2O2. Mole weight: 176.17. |  |
| Acetyl-L-lysine | Acetyl-L-lysine is an acetylated form of the amino acid L-lysine. Acetyl-L-lysine can participate in protein acylation processes, affecting protein functions such as stability and enzyme activity [1]. Uses: Scientific research. Group: Natural products. CAS No. 1946-82-3. Pack Sizes: 10 mM * 1 mL; 100 mg; 500 mg. Product ID: HY-W048838. | |
| Allyl D-Glucuronate-13C6 | Labeled Allyl D-Glucuronate. It is used in efficient synthesis of 1 β-O-acyl glucuronides via regioselective acylation of allyl or benzyl D-glucuronate. Group: Biochemicals. Alternative Names: D-Glucopyranuronic Acid-13C6 2-Propen-1-yl Ester; D-Glucuronic Acid-13C6 2-Propenyl Ester. Grades: Highly Purified. Pack Sizes: 1mg. US Biological Life Sciences. | Worldwide |
| Aluminum Chloride | Aluminum Trichloride is a powerful chemical reagent used as a catalyst in Freidel Crafts reactions, alkylations and acylations. Group: Biochemicals. Alternative Names: Aluminum(III) Chloride; Hemogin L; Hemostop; Lutan FN; NSC 143015; NSC 143016;TK Flock; Takibine 100; Trichloroaluminum; Aluminium Chloride; Aluminium Trichloride; AlCl3. Grades: Highly Purified. CAS No. 7446-70-0. Pack Sizes: 100g, 250g, 500g. Molecular Formula: AlCl3. US Biological Life Sciences. | Worldwide |
| Aluminum trifluoromethanesulfonate | Friedel-Crafts Reactions. Aluminum trifluoromethanesulfonate has been used for the Friedel-Crafts alkylation reaction of toluene with isopropyl and tert-butyl chlorides (eq 1), and for theacylationof Benzene andtoluenewithacetylandbenzoylchlo- rides in low to moderate yields. Intramolecular Friedel-Crafts acylation of an aromatic compound with Meldrum's acid has also been reported using catalytic amounts of Al(OTf) 3. Acylation of 2-methoxynaphthalene with acetic anhydride has been reported using Al(OTf) 3 and lithium perchlorate as an additive to afford the corresponding 6-acetylated adduct in 83% yield. Effective acylation of arenes with carboxylic acids has also been disclosed using polystyrene-supported Al(OTf)3. Group: Organic aluminium. Alternative Names: Aluminum triflate. CAS No. 74974-61-1. Molecular formula: C3AlF9O9S3. Mole weight: 474.2. Appearance: Powder. Purity: 0.99. IUPACName: aluminum;trifluoromethanesulfonate. Canonical SMILES: C(F)(F)(F)S(=O)(=O)[O-]. C(F)(F)(F)S(=O)(=O)[O-]. C(F)(F)(F)S(=O)(=O)[O-]. [Al+3]. Catalog: ACM74974611-1. | |
| Arachidonoyl coenzyme A lithium salt | Arachidonoyl coenzyme A lithium salt is a substrate for the long-chain N-acylation of glycines by enzymes such as glycine N-acyltransferase-like 2 (GLYATL2) and of acytransferases such as lysophosphatidic acid acyltransferase (CGI-58/ABHD5). Arachidonoyl CoA is used as a charged membrane-impermeant analog of arachidonic acid (AA). Arachidonoyl CoA is used in the synthesis of arachidonoyl amino acids by cytochrome c. Applications: A substrate for the long-chain n-acylation of glycines by enzymes such as glyatl2. Group: Coenzymes. Synonyms: cis,cis,cis,cis-5,8,11,14-Eicosatetraenoyl coenzyme A lithium salt. CAS No. 188174-63-2. Purity: ≥85%. Mole weight: 1059.92. Appearance: Powder. Form: Solid. cis,cis,cis,cis-5,8,11,14-Eicosatetraenoyl coenzyme A lithium salt; Arachidonoyl coenzyme A lithium salt; 188174-63-2. Cat No: COEC-030. |  |
| aspartoacylase | Aspartoacylase (EC 3.5.1.15, aminoacylase II, N-acetylaspartate amidohydrolase, acetyl-aspartic deaminase, acylase II, ASPA) is a hydrolase enzyme responsible for catalyzing the deacylation of N-acetyl-l-aspartate (N-acetylaspartate,NAA) into aspartate and acetate. It is a zinc-dependent hydrolase that promotes the deprotonation of water to use as a nucleophile in a mechanism analogous to many other zinc-dependent hydrolases. It is most commonly found in the brain, where it controls the levels of N-actetyl-l-aspartate. Group: Enzymes. Synonyms: aminoacylase II; N-acetylaspartate amidohydrolase; acetyl-aspartic deaminase; acylase II. Enzyme Commission Number: EC 3.5.1.15. CAS No. 9031-86-1. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-4404; aspartoacylase; EC 3.5.1.15; 9031-86-1; aminoacylase II; N-acetylaspartate amidohydrolase; acetyl-aspartic deaminase; acylase II. Cat No: EXWM-4404. | |
| Bis (dibenzylideneacetone)palladium (0) | Bis (dibenzylideneacetone)palladium (0). Uses: Palladium-catalyzed acylation of unsaturated halides by anions of enol ethers. asymmmetric allylation reactions. intramolecular reactions with alkenes. carbonylation reactions. cross coupling reactions. Group: Salt. Alternative Names: CB-706; MFCD00051942; Bis (dibenzylideneacetone)palladium (0); (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one,palladium; GC10019; RW2139; bis(dibenzylidene-acetone)palladium; bis (dibenzylideneacetone)palladium; PubChem14428; J-400823. CAS No. 32005-36-0. Product ID: (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one; palladium. Molecular formula: 575.016g/mol. Mole weight: C34H28O2Pd. C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. [Pd]. InChI=1S/2C17H14O. Pd/c2*18-17 (13-11-15-7-3-1-4-8-15) 14-12-16-9-5-2-6-10-16; /h2*1-14H; /b2*13-11+, 14-12+;. UKSZBOKPHAQOMP-SVLSSHOZSA-N. | |
| Bis (dibenzylideneacetone)palladium (0) | Palladium-catalyzed acylation of unsaturated halides by anions of enol ethers. Asymmmetric Allylation reactions. Intramolecular reactions with alkenes. Carbonylation reactions. Cross Coupling reactions. Group: Palladium series catalysts. Alternative Names: CB-706; MFCD00051942; Bis (dibenzylideneacetone)palladium (0); (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one,palladium; GC10019; RW2139; bis(dibenzylidene-acetone)palladium; bis (dibenzylideneacetone)palladium; PubChem14428; J-400823. CAS No. 32005-36-0. Molecular formula: C34H28O2Pd. Mole weight: 575.016g/mol. IUPACName: (1E,4E)-1,5-diphenylpenta-1,4-dien-3-one;palladium. Canonical SMILES: C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. C1=CC=C(C=C1)C=CC(=O)C=CC2=CC=CC=C2. [Pd]. ECNumber: 608-691-6. Catalog: ACM32005360. | |
| CCA tRNA nucleotidyltransferase | The acylation of all tRNAs with an amino acid occurs at the terminal ribose of a 3' CCA sequence. The CCA sequence is added to the tRNA precursor by stepwise nucleotide addition performed by a single enzyme that is ubiquitous in all living organisms. Although the enzyme has the option of releasing the product after each addition, it prefers to stay bound to the product and proceed with the next addition. Group: Enzymes. Synonyms: CCA-adding enzyme; tRNA adenylyltransferase; tRNA cytidylyltransferase; tRNA CCA-pyrophosphorylase; tRNA-nucleotidyltransferase; transfer-RNA nucleotidyltransferase; transfer ribonucleic acid nucleotidyl transferase; C. Enzyme Commission Number: EC 2.7.7.72. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-3284; CCA tRNA nucleotidyltransferase; EC 2.7.7.72; CCA-adding enzyme; tRNA adenylyltransferase; tRNA cytidylyltransferase; tRNA CCA-pyrophosphorylase; tRNA-nucleotidyltransferase; transfer-RNA nucleotidyltransferase; transfer ribonucleic acid nucleotidyl transferase; CTP(ATP):tRNA nucleotidyltransferase; transfer ribonucleate adenylyltransferase; transfer ribonucleate adenyltransferase; transfer RNA adenylyltransferase; transfer ribonucleate nucleotidyltransferase; ATP (CTP):tRNA nucleotidyltransferase; ribonucleic cytidylic cytidylic | |
| Cerium Chloride Anhydrous | Cerium Chloride, in forms of crystalline aggregates or lHight yellow lump aggregates, is the important material for catalyst, glass, phosphors and polishing powders. It is also used to decolorize glass by keeping iron in its ferrous state. The ability of Cerium-doped glass to block out ultra violet lHight is utilized in the manufacturing of medical glassware and aerospace windows. It is also used to prevent polymers from darkening in sunlHight and to suppress discoloration of television glass. It is applied to optical components to improve performance. Uses: Used as petroleum catalyst, automobile exhaust catalysts, organic synthesis catalyst, pharmaceutical intermediates, also used as a starting point for the preparation of other cerium salts, such as the lewis acid, cerium(iII) trifluoromethanesulfonate, used for friedel-crafts acylations. it can be used itself as a lewis acid, for example as a catalyst in friedel-crafts alkylation reactions. Group: Ce. CAS No. 779008-60-5. Molecular formula: CeCl3. Mole weight: 246g/mol. Appearance: White crystalline. Density: 3.92g/mL. Catalog: ACM779008605. | |
| Cerulenin (2,3-Epoxy-4-oxo-7,10-dodecadienamide) | Antibiotic. Fatty acid synthase (FAS) inhibitor, reported to bind in equimolar ratio to B-keto-acyl- ACP synthase, thus inhibiting protein acylation. Produces metabolic effects similar to effects of leptin, but through mechanisms that are independent of, or down-stream from, both leptin and melanocortin receptors. Apoptosis inducer. Inhibitor of bacterial fatty acid synthesis (inhibits FabH, FabB and FabF condensation enzymes). Group: Biochemicals. Grades: Highly Purified. CAS No. 17397-89-6. Pack Sizes: 5mg. Molecular Formula:C12H17NO3 MOLECULAR WEIGHT: 223.3. US Biological Life Sciences. | Worldwide |
| Chloramphenicol succinate | Prepared by acylation of chloramphenicol with succinic anhydride to provide a water soluble pro-drug; represents an alternative prodrug strategy for chloramphenicol that has found a niche in surface antibiotic treatment in surgery; acts as a prodrug, forming chloramphenicol in the presence of succinate dehydrogenase. Synonyms: Kemicetine. Grades: >99% by HPLC. CAS No. 3544-94-3. Molecular formula: C15H16Cl2N2O8. Mole weight: 423.20. | |
| Chlorotrityl Polystyrene, Type1 | Chlorotrityl Polystyrene, Type1. Uses: This highly acid labile resin is useful for the immobilization of alcohols, amines and carboxylic acids. cleavage is in general achieved by using either 1-5% tfa in ch2cl2 (containing 5% triisopropylsilane) or acetic acid. this resin can also be used in fmoc peptide synthesis under basic acylation conditions. carboxylic acids can be released under very mild acidic conditions by treatment with acoh/tfe/dcm or hfip in dcm. completely protected peptides are generated under this conditions. Group: Chlorotrityl polystyrene resins. Alternative Names: Trityl Chloride Resin. Pack Sizes: 5g, 25g, 100g. | |
| Chlorotrityl Polystyrene, Type2 | Chlorotrityl Polystyrene, Type2. Uses: This highly acid labile resin is useful for the immobilization of alcohols, amines and carboxylic acids. cleavage is in general achieved by using either 1-5% tfa in ch2cl2 (containing 5% triisopropylsilane) or acetic acid. this resin can also be used in fmoc peptide synthesis under basic acylation conditions. carboxylic acids can be released under very mild acidic conditions by treatment with acoh/tfe/dcm or hfip in dcm. completely protected peptides are generated under this conditions. Group: Chlorotrityl polystyrene resins. Alternative Names: Trityl Chloride Resin. Pack Sizes: 5g, 25g, 100g. | |
| Chlorotrityl Polystyrene, Type3 | Chlorotrityl Polystyrene, Type3. Uses: This highly acid labile resin is useful for the immobilization of alcohols, amines and carboxylic acids. cleavage is in general achieved by using either 1-5% tfa in ch2cl2 (containing 5% triisopropylsilane) or acetic acid. this resin can also be used in fmoc peptide synthesis under basic acylation conditions. carboxylic acids can be released under very mild acidic conditions by treatment with acoh/tfe/dcm or hfip in dcm. completely protected peptides are generated under this conditions. Group: Chlorotrityl polystyrene resins. Alternative Names: Trityl Chloride Resin. Pack Sizes: 5g, 25g, 100g. | |
| Dimethyl-pyridin-4-yl-amine (DMAP) | Dimethyl-pyridin-4-yl-amine is a highly efficient catalyst for acylation reactions. Uses: A highly efficient catalyst for acylation reactions. Synonyms: 4-(dimethylamino)-pyridin; 4-Dimethylaminepyridine; gamma-(Dimethylamino)pyridine; N,N-Dimethyl-4-aminopyridine; n,n-dimethyl-4-pyridinamin; p-Dimethylaminopyridine; Pyridine, 4-(dimethylamino)-; AURORA KA-6495; DMAP; 4-dimethylaminopyridine; 4-DMAP; γ-(Dimethylamino)pyridine; USP Valacyclovir Related Compound G; Valaciclovir EP Impurity G; Valacyclovir USP Related Compound G. Grades: 98%. CAS No. 1122-58-3. Molecular formula: C7H10N2. Mole weight: 122.17. | |
| Diphenyl ether | Diphenyl ether is the organic compound with the formula O(C6H5)2. The molecule is subject to reactions typical of other phenyl rings, including hydroxylation, nitration, halogenation, sulfonation, and Friedel - Crafts alkylation or acylation. This simple diaryl ether enjoys a variety of niche applications. Group: Ethers. Alternative Names: Diphenyl oxide. CAS No. 101-84-8. Molecular formula: C12H10O. Mole weight: 170.21. Appearance: Clear pale yellowish liquid after melting. Purity: 98%+. IUPACName: Phenoxybenzene. Canonical SMILES: C1=CC=C(C=C1)OC2=CC=CC=C2. Density: 1.073 g/mL at 25 °C(lit.). ECNumber: 202-981-2. Catalog: ACM101848. | |
| Fmoc-(Dmb)Gly-OH | Fmoc-(Dmb)Gly-OH is an excellent reagent for enhancing synthetic efficiency of glycine-containing peptides by Fmoc SPPS.Like the analogous Hmb derivative Fmoc-(FmocHmb)Gly-OH, the use of this derivative prevents aggregation during chain assemby, thereby leading to faster and more predictable acylation and deprotection reactions. Furthermore, it can prevent aspartimide formation when used to introduce a Gly immediately before an Asp residue and help promote cyclization of Gly-containing peptides. The analogous (Tmob)Gly derivative has been used by Bayer and colleagues to prepare a 64-residue transmembrane peptide in remarkable purity. Uses: Peptide synthesis. Group: Amino acids. Alternative Names: Fmoc-(Dmb)Gly-OH, N-α-Fmoc-N-α-(2, 4-dimethoxybenzyl)-glycine. CAS No. 166881-42-1. Mole weight: 447.48. Catalog: ACM166881421. | |
| Immobilized Lipase B from Candida antarctica, Recombinant | Recombinant Lipase B from Candida antarctica (CALB) is produced by submerged fermentation with genetically modified Pichia pastoris. CALB can be used in the water phase or organic phase catalytic esterification, esterolysis, transesterification, ring opening polyester synthesis, aminolysis, hydrolysis of amides, acylation of amines and addition reaction. CALB is with high chiral selectivity and position selectivity, so it can be widely used in oil processing, food, medicine, cosmetic and other chemical industries.CALB is immobilized by physical adsorption on the highly hydrophobic resin that is a macroporous, styrene/methacrylate polymer. Applications: Immobilized calb is suitable for applications in organic solvents and solvent-free systems, and can be recycled and reused for much times in suitable conditions. Group: Enzymes. Synonyms: Lipase B; Immobilized Lipase B; Immobilized CALB; CALB; Immobilized Lipase; Immobilized; Lipase. Lipase. Source: Pichia pastoris. Species: Candida antarctica. Lipase B; Immobilized Lipase B; Immobilized CALB; CALB; Immobilized Lipase; Immobilized; Lipase. Cat No: NATE-1897. | |
| indoleacetylglucose-inositol O-acyltransferase | The position of acylation is indeterminate because of the ease of acyl transfer between hydroxy groups. Group: Enzymes. Synonyms: indole-3-acetyl-β-1-D-glucoside:myo-inositol indoleacetyltransferase; 1-O-(indol-3-ylacetyl)-β-D-glucose:myo-inositol indole-3-ylacetyltransferase. Enzyme Commission Number: EC 2.3.1.72. CAS No. 74082-57-8. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2252; indoleacetylglucose-inositol O-acyltransferase; EC 2.3.1.72; 74082-57-8; indole-3-acetyl-β-1-D-glucoside:myo-inositol indoleacetyltransferase; 1-O-(indol-3-ylacetyl)-β-D-glucose:myo-inositol indole-3-ylacetyltransferase. Cat No: EXWM-2252. | |
| indolylacetylinositol arabinosyltransferase | The position of acylation is indeterminate because of the ease of acyl transfer between hydroxy groups. For a diagram showing the biosynthesis of UDP-L-arabinose, click here. Group: Enzymes. Synonyms: arabinosylindolylacetylinositol synthase; UDP-L-arabinose:indol-3-ylacetyl-myo-inositol L-arabinosyltransferase; UDP-L-arabinose:(indol-3-yl)acetyl-myo-inositol L-arabinosyltransferase. Enzyme Commission Number: EC 2.4.2.34. CAS No. 84720-96-7. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2662; indolylacetylinositol arabinosyltransferase; EC 2.4.2.34; 84720-96-7; arabinosylindolylacetylinositol synthase; UDP-L-arabinose:indol-3-ylacetyl-myo-inositol L-arabinosyltransferase; UDP-L-arabinose:(indol-3-yl)acetyl-myo-inositol L-arabinosyltransferase. Cat No: EXWM-2662. | |
| LacK free acid | LacK (free acid) is a lysine derivative used in lactate acylation studies [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 1227379-69-2. Pack Sizes: 5 mg; 10 mg; 25 mg; 50 mg; 100 mg. Product ID: HY-W883690. | |
| Lipase A from Candida Antarctica, Recombinant | Lipase A from Candida Antarctica catalyzes hydrolysis of tertiary alcohols to form glycerol and fatty acids and shows selectivity for the N-acylation of β-amino esters. Group: Enzymes. Synonyms: EC 3.1.1.3; lipase; triglyceride lipase; tributyrase; butyrinase; glycerol ester hydrolase; tributyrinase; Tween hydrolase; steapsin; triacetinase; tributyrin esterase; Tweenase; amno N-AP; Takedo 1969-4-9; Meito . Enzyme Commission Number: EC 3.1.1.3. CAS No. 9001-62-1. Lipase. Activity: ~2 units/mg. Storage: 2-8°C. Form: powder; beige. Source: Aspergillus oryzae. Species: Candida Antarctica. EC 3.1.1.3; lipase; triglyceride lipase; tributyrase; butyrinase; glycerol ester hydrolase; tributyrinase; Tween hydrolase; steapsin; triacetinase; tributyrin esterase; Tweenase; amno N-AP; Takedo 1969-4-9; Meito MY 30; Tweenesterase; GA 56; capalase L; triglyceride hydrolase; triolein hydrolase; tween-hydrolyzing esterase; amano CE; cacordase; triglyceridase; triacylglycerol ester hydrolase; amano P; amano AP; PPL; glycerol-ester hydrolase; GEH; meito Sangyo OF lipase; hepatic lipase; lipazin; post-heparin plasma protamine-resistant lipase; salt-resistant post-heparin lipase; heparin releasable hepatic lipase; amano CES; amano B; tributyrase; triglyceride lipase; liver lipase; hepatic monoacylglycerol acyltransferase; 9001-62-1. Cat No: NATE-0397. | |
| Lysophosphatidylethanolamines, egg | Lysophosphatidylethanolamine (LPE) is a naturally-occurring lysophospholipid that can be generated via deacylation of phosphatidylethanolamine by phospholipase A2 (PLA2). It increases the phosphorylation of ERK1/2 in PC12 cells, an effect that can be blocked by the MEK inhibitors U-0126 (HY-12031A) and PD 98059 (HY-12028) and the EGFR inhibitor AG-1478 (HY-13524).1 LPE also increases neurite outgrowth and expression of neurofilament M in PC12 cells. LPE inhibits the activity of phospholipase D (PLD) partially purified from cabbage.3 This product contains lysophosphatidylethanolamine molecular species with variable fatty acyl chain lengths at the sn-1 position and a hydroxy group at the sn-2 position. Uses: Scientific research. Group: Signaling pathways. Alternative Names: Lyso-PE (egg); LPE (egg); L-α-lysophosphatidylethanolamine. CAS No. 97281-40-8. Pack Sizes: 1 mg; 5 mg. Product ID: HY-156041. | |
| NAI-N3 | NAI-N3 is a novel RNA acylation reagent that enables RNA purification. Synonyms: [2-(azidomethyl)pyridin-3-yl]-imidazol-1-ylmethanone. CAS No. 1612756-29-2. Molecular formula: C10H8N6O. Mole weight: 228.21. | |
| NAI-N3 | NAI-N3 is a probe for icSHAPE (in vivo click selective 2'-hydroxyl acylation and profiling experiment). It acylates the 2'-OH in ssRNA and enables RNA structure profiling in vivo and ex vivo for all four bases. NAI-N3 can be used for site-specific RNA acylation using the RAIL (RNA Acylation at Induced Loops) method or in Apta-Seq to discover new aptamers in selected pools. Group: Others. Alternative Names: NAI-N3; NAIN3; NAI N3. CAS No. 1612756-29-2. Molecular formula: C10H8N6O. Mole weight: 228.22. Appearance: Solid powder. Purity: >98%. IUPACName: (2-(azidomethyl)pyridin-3-yl)(1H-imidazol-1-yl)methanone. Canonical SMILES: [N-]=[N+]=NCC1=C (C=CC=N1)C (N2C=CN=C2)=O. Catalog: ACM1612756292. | |
| Native Pseudomonas sp. Sphingolipid ceramide N-deacylase | Sphingolipid ceramide N-deacylase (SCDase) is derived from Pseudomonas and hydrolyzes the N-acyl linkage between fatty acids and sphingosine bases in ceramides of various sphingolipids. The enzyme also catalyzes the reverse reaction and possesses transacylation activity. SCDase acts on various acidic and neutral glycosphingolipids and sphingomyelin; however, it exhibits low activity with ceramides. Applications: Hydrolysis of n-acyl linkages between fatty acids and sphingosine bases sphingolipid hydrolysis. Group: Enzymes. Synonyms: SCDase; Sphingolipid ceramide N-deacylase. SCDase. Storage: Store at -20°C until use. Store reconstituted solution in aliquots at -20°C. Avoid freeze-thaw. Form: Solution in 50 mM sodium acetate (pH 6.0) containing 0.1% Lubrol PX. Source: Pseudomonas sp. Species: Pseudomonas sp. SCDase; Sphingolipid ceramide N-deacylase. Cat No: NATE-0896. | |
| N,N-Dimethylsphingosine ((2S,3R,4E)-2-(Dimethylamino)-4-octadecene-1,3-diol) | Competitive sphingosine kinase (SphK) inhibitor. Exhibits inhibitory activity in platelets and in cytosolic extracts from U937, Swiss 3T3 and PC12 cells. Selectively inhibits sphingosine phosphorylation; does not inhibit N-acylation, and displays no inhibitory effect on protein kinase C at concentrations that inhibit SphK. Increases the release of IL-1beta and MCP-1 in cultured astrocytes; thought to mediate mechanical allodynia via this mechanism. Group: Biochemicals. Grades: Highly Purified. CAS No. 119567-63-4. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| (R)-(+)-1-(4-Chlorophenyl)ethylamine | 1-(4-Chlorophenyl)ethylamine is a chiral amine that may be used in the preparation of N-phenylacetyl-(R)-1-(4-chlorophenyl)ethylamine via enantioselective acylation in aqueous medium and in the presence of penicillin acylase from Alcaligenes faecalis. Uses: (r)-(+)-1-(4-chlorophenyl)ethylamine, is used as an important raw material and intermediate used in organic synthesis, pharmaceuticals, agrochemicals and dyestuff. it is used as a chiral reagent. Group: Solvents. Alternative Names: (1R)-1-(4-Chlorophenyl)ethanamine Benzenemethanamine, 4-chloro-α-methyl-, (αR)- Benzenemethanamine, 4-chloro-α-methyl- 1-(4-Chlorophenyl)ethanamine. CAS No. 27298-99-3. Molecular formula: C8H10ClN. Mole weight: 155.63. IUPACName: 1-(4-chlorophenyl)ethan-1-amine. Canonical SMILES: CC(N)C1=CC=C(Cl)C=C1. Density: 1.1±0.1 g/cm3. Catalog: ACM27298993. | |
| RU-SKI 43 hydrochloride | RU-SKI 43 is a potent and selective inhibitor of Hedgehog acyltransferase (HHAT). It blocks palmitoylation of Shh without affecting palmitoylation of H-Ras or Fyn, myristoylation of c-Src, or acylation of Wnt3a. Synonyms: 2-(2-methylbutylamino)-1-[4-[(3-methylphenoxy)methyl]-6,7-dihydro-4H-thieno[3,2-c]pyridin-5-yl]ethanone hydrochloride. Grades: ≥98%. CAS No. 1782573-67-4. Molecular formula: C22H30N2O2S·HCl. Mole weight: 423. | |
| Scandium(III) triflate | Water tolerant Lewis acid. Commonly used in a range of Lewis acid catalyzed reactions. Efficient metal source for Lewis acid catalyzed asymmetric reactions. Catalyzes Friedel-Crafts alkylation, acylation and related reactions. Catalyzes various domino- and multi-component processes. Catalyzes electrophilic additions of alpha-diazoesters with ketones. Catalyzes carbon insertion reactions. Group: Scandium catalysts. Alternative Names: Scandium(III) trifluoromethanesulfonate; KSC174E3P; KS-000002BK; Trifluoromethanesulfonic acid scandium(III) salt; ACT08645; RTR-005607; SCANDIUM TRIS(TRIFLUOROMETHANESULFONATE); SC(SO3CF3)3; scandium(3+); scandium (III)trifluoromethanesulfonate. CAS No. 144026-79-9. Molecular formula: C3F9O9S3Sc. Mole weight: 492.16 g/mol. IUPACName: scandium(3+); trifluoromethanesulfonate. Canonical SMILES: C(F)(F)(F)S(=O)(=O)[O-]. C(F)(F)(F)S(=O)(=O)[O-]. C(F)(F)(F)S(=O)(=O)[O-]. [Sc+3]. Catalog: ACM144026799. | |
| Trifluoromethanesulfonic acid silver | Trifluoromethanesulfonic acid (Triflic acid) silver, a perfluoroalkanesulfonic acid, is one of the superior catalysts for C- or O-acylation [1]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: Triflic acid silver; Perfluoromethanesulfonic acid silver; Fluorad FC 24 silver. CAS No. 2923-28-6. Pack Sizes: 10 g; 25 g. Product ID: HY-W020983. | |
| Tri-tert-butylphosphonium tetrafluoroborate | Air-stable, non-pyrophoric precursor of the Tri-t-butylphosphine ligand which is used in a variety of catalytic processes. Ligand for Suzuki cross-couplings. Ligand for Heck Reactions. Ligand for Stille Cross-couplings. Ligand for α-Arylation and vinylation of arylmandelic acid derivatives. Ligand for direct arylation of hetercycles Synthesis of benzocyclobutenes by C-H activation. Cross-coupling of Grignard reagents and aryl bromides. Palladium catalyzed annulation of haloanilines. Palladium-Catalyzed Acylation. Palladium Catalyzed Carbonylative Heck Reaction. Palladium-catalyzed aminosulfonylation. Palladium-catalyzed intramolecular C-O bond formation. Ruthenium-catalyzed cross-coupling of aldehydes with arylboronic acid. Group: Borate. Alternative Names: Fluoroboric Acid Tri-Tert-Butylphosphine Adduct. CAS No. 131274-22-1. Molecular formula: C12H28BF4P. Mole weight: 290.13. Appearance: Solid. Purity: 0.98. IUPACName: tritert-butylphosphanium;tetrafluoroborate. Canonical SMILES: [B-](F)(F)(F)F. CC(C)(C)[PH+](C(C)(C)C)C(C)(C)C. Catalog: ACM131274221-1. | |
| 04:1 Coenzyme A Sodium salt | 04:1 Coenzyme A Sodium salt is a fundamental biochemical compound prevalent in the biomedical sector, demonstrating its indispensability as a coenzyme involved in diverse metabolic pathways. Its remarkable functionality aids in the seamless transfer of acyl groups. Moreover, owing to its profound impact on lipid metabolism, this product emerges as a potential solution in the treatment of metabolic afflictions, including obesity, diabetes, and cardiovascular anomalies. Synonyms: (E)-but-2-enoyl Coenzyme A (sodium salt); sodium (2R, 3S, 4R, 5R) -5- (6-amino-9H-purin-9-yl) -2- ( ( ( ( ( ( (R) -4- ( (3- ( (2- ( ( (E) -but-2-enoyl) thio) ethyl) amino) -3-oxopropyl) amino) -3-hydroxy-2, 2-dimethyl-4-oxobutoxy) oxidophosphoryl) oxy) oxidophosphoryl) oxy) methyl) -4-hydroxytetrahydrofuran-3-yl hydrogen phosphate; 9H-Purin-6-amine, 9- [ (2ξ ) -5-O- [hydroxy [ [hydroxy [ (3R) -3-hydroxy-2, 2-dimethyl-4-oxo-4- [ [3-oxo-3- [ [2- [ [ (2E) -1-oxo-2-buten-1-yl] thio] ethyl] amino] propyl] amino] butoxy] phosphinyl] oxy] phosphinyl] -3-O-phosphono-β -D-threo-pentofuranosyl] -, sodium salt (1:3). Grades: >99%. CAS No. 2260670-60-6. Molecular formula: C25H37N7Na3O17P3S. Mole weight: 901.55. | |
| 10-deacetylbaccatin III 10-O-acetyltransferase | The enzyme will not acylate the hydroxy group at 1β, 7β or 13α of 10-deacetyl baccatin III, or at 5α of taxa-4(20),11-dien-5α-ol. May be identical to EC 2.3.1.163, 10-hydroxytaxane O-acetyltransferase. Group: Enzymes. Enzyme Commission Number: EC 2.3.1.167. CAS No. 220946-63-4. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2107; 10-deacetylbaccatin III 10-O-acetyltransferase; EC 2.3.1.167; 220946-63-4. Cat No: EXWM-2107. | |
| 10-deoxymethynolide synthase | The product, 10-deoxymethynolide, contains a 12-membered ring and is an intermediate in the biosynthesis of methymycin in the bacterium Streptomyces venezuelae. The enzyme also produces narbonolide (see EC 2.3.1.240, narbonolide synthase). The enzyme has 29 active sites arranged in four polypeptides (pikAI - pikAIV) with a loading domain, six extension modules and a terminal thioesterase domain. Each extension module contains a ketosynthase (KS), keto reductase (KR), an acyltransferase (AT) and an acyl-carrier protein (ACP). Not all active sites are used in the biosynthesis. Group: Enzymes. Synonyms: pikromycin PKS. Enzyme Commission Number: EC 2.3.1.239. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2187; 10-deoxymethynolide synthase; EC 2.3.1.239; pikromycin PKS. Cat No: EXWM-2187. | |
| 1-[1-[-2-[tert-Butyldimethylsilyloxy]-1-hydroxy-1-methyl-4-(trimethylsilyl)-3-butynyl]cyclopropyl]-ethanone | Intermediate in the synthesis of Acylfulvene derivative antitumor agents. Group: Biochemicals. Alternative Names: 1-[1-[-2-[[ (1, 1-Dimethylethyl) dimethylsilyl]oxy]-1-hydroxy-1-methyl-4- (trimethylsilyl) -3-butynyl]cyclopropyl]-ethanone. Grades: Highly Purified. Pack Sizes: 100mg. US Biological Life Sciences. | Worldwide |
| 1,1'-Carbonyldi(1,2,4-triazole) | It is used in epoxidation reactions in organic synthesis. It is useful in preparing acyl triazolides from carboxylic acids. Synonyms: CDT; 1,1'-Carbonyl-di-(1,2,4-triazole). Grades: ≥ 98% (Titration). CAS No. 41864-22-6. Molecular formula: C5H4N6O. Mole weight: 164.13. | |
| 1,1-Cyclohexanediacetic Anhydride | 1,1-Cyclohexanediacetic Anhydride is a building block used as a reagent in the synthesis of N-acylanthranilic acid derivatives as plasminogen activator inhibitor-1 inhibitors with good oral bioavailability. Group: Biochemicals. Grades: Highly Purified. CAS No. 1010-26-0. Pack Sizes: 1g, 5 g. Molecular Formula: C10H14O3, Molecular Weight: 182.22. US Biological Life Sciences. | Worldwide |
| 11-Hydroxy Myristic Acid | A possible fatty acyl pheromone precursors in Spodoptera littoralis. Group: Biochemicals. Alternative Names: 11-Hydroxytetradecanoic Acid. Grades: Highly Purified. CAS No. 2034-56-2. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| 11-Hydroxy Myristic Acid | A possible fatty acyl pheromone precursors in Spodoptera littoralis. Group: Heterocyclic organic compound. Alternative Names: 11-Hydroxytetradecanoic Acid. CAS No. 2034-56-2. Molecular formula: C14H28O3. Mole weight: 244.37. Purity: 0.96. IUPACName: 11-hydroxytetradecanoic acid. Canonical SMILES: CCCC(CCCCCCCCCC(=O)O)O. Density: 0.969g/cm³. Catalog: ACM2034562. | |
| (11Z)-hexadec-11-enoyl-CoA conjugase | The enzyme, characterized from the silk moth Bombyx mori, catalyses a step in the pathway for the biosynthesis of bombykol, a sex pheromone produced by the moth. The enzyme converts a single cis double bond at position 11 of (11Z)-hexadec-11-enoyl-CoA into conjugated 10 trans and 12 cis double bonds. Prior to catalysing this reaction, the enzyme catalyses the introduction of the cis bond in position 11 (cf. EC 1.14.19.5, acyl-CoA 11-desaturase). Group: Enzymes. Synonyms: Bmpgdesat1 (gene name). Enzyme Commission Number: EC 1.14.19.15. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-0977; (11Z)-hexadec-11-enoyl-CoA conjugase; EC 1.14.19.15; Bmpgdesat1 (gene name). Cat No: EXWM-0977. | |
| 1,2,3,4-Tetrahydro-2-naphthoic Acid | 1,2,3,4-Tetrahydro-2-naphthoic Acid is used as a reagent in organic synthesis of several compounds including that of N-acyl-5-methyl-3(2H)-isoxazolone derivatives which show high potential as fungicides. Group: Biochemicals. Grades: Highly Purified. CAS No. 53440-12-3. Pack Sizes: 100mg, 1g. Molecular Formula: C11H12O2, Molecular Weight: 176.21. US Biological Life Sciences. | Worldwide |
| 1,2,5-Tri-O-benzoyl-3-methyl-D-xylofuranose | 1-O-acyl-2,3,5-tri-O-benzoyl-D-xylofuranose, commonly known as 1,2,5-Tri-O-benzoyl-3-methyl-D-xylofuranose, is a multifunctional organic compound frequently employed in the challenging synthesis of various carbohydrate derivatives. Its outstanding configuration and reactivity make it a valuable building block for the preparation of natural products and tailored pharmaceutical agents. By introducing novel functional groups onto its framework, it is possible to potentially design drugs that exhibit enhanced bioavailability, improved efficacy, and reduced toxicity towards the treatment of some of the most common and life-threatening maladies, such as diabetes, cancer, and neurological disorders. Molecular formula: C27H24O7. Mole weight: 460.48. | |
| (-)-1,2-Bis((2R,5R)-2,5-diphenylphospholano)ethane(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate, min. 98% (R,R)-Ph-BPE-Rh | 1. Phenyl-BPE exhibits enhanced activity and selectivity over existing members of the BPE ligand family in rhodium catalysed asymmetric hydrogenation. 2. This ligand is highly efficient for the hydrogenation of N-acyl aryl-enamides. 3. Molar substrate/catalyst ratios of up to 100,000/1 are achieved with excellent reactivity and enantioselectivity using commercial grade substrates and solvents. 4. Ligand in the rhodium-catalyzed asymmetric hydroformylation of olefins. Group: Heterocyclic organic compound. Alternative Names: 528565-84-6;1,2-Bis[(2R,5R)-2,5-diphenylphospholano]ethane(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate;(R,R)-Ph-BPE-Rh;(-)-1,2-Bis((2R,5R)-2,5-diphenylphospholano)ethane(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate; MFCD07369037; DTXSID20746256; PUBCHEM_71310600; (-)-1, 2-Bis ( (2R, 5R)-2, 5-diphenylphospholano)ethane (1, 5-cyclooctadiene)rhodium (I)tetrafluoroborate. CAS No. 528565-84-6. Molecular formula: C42H48BF4P2Rh-. Mole weight: 804.503g/mol. IUPACName: (1Z, 5Z)-cycloocta-1, 5-diene; (2R, 5R)-1-[2-[(2R, 5R)-2, 5-diphenylphospholan-1-yl]ethyl]-2, 5-diphenylphospholane; rhodium; tetrafluoroborate. Canonical SMILES: [B-] (F) (F) (F) F. C1CC=CCCC=C1. C1CC (P (C1C2=CC=CC=C2) CCP3C (CCC3C4=CC=CC=C4) C5=CC=CC=C5) C6=CC=CC=C6. [Rh]. Catalog: ACM528565846. | |
| (+)-1,2-Bis((2S,5S)-2,5-diphenylphospholano)ethane(1,5-cyclooctadiene)rhodium(I) tetrafluoroborate, min. 98% (S,S)-Ph-BPE-Rh | Phenyl-BPE exhibits enhanced activity and selectivity over existing members of the BPE ligand family in rhodium catalysed asymmetric hydrogenation. This ligand is highly efficient for the hydrogenation of N-acyl aryl-enamides. Molar substrate/catalyst ratios of up to 100,000/1 are achieved with excellent reactivity and enantioselectivity using commercial grade substrates and solvents. Ligand in the rhodium-catalyzed asymmetric hydroformylation of olefins. Group: Rhodium catalysts. Alternative Names: 849950-53-4; (S, S)-Ph-BPE-Rh; DTXSID60746255; PUBCHEM_71310599; MFCD07369038; (+)-1, 2-Bis (2S, 5S)-2, 5-diphenylphospholano)ethane- (1, 5-cyclooctadiene)rhodium (I)tetrafluoroborate; 1, 2-Bis[ (2S, 5S)-2, 5-diphenylphospholano]ethane (1, 5-cyclooctadiene)rhodium (I) tetrafluoroborate;1,2-Bis[(s,s)-2,5-diphenylphospholano]ethane-(1,5-cycloocta-diene)rhodium(I)tetrafluoroborate. CAS No. 849950-53-4. Molecular formula: C42H48BF4P2Rh-. Mole weight: 804.503g/mol. IUPACName: (1Z, 5Z)-cycloocta-1, 5-diene; (2S, 5S)-1-[2-[(2S, 5S)-2, 5-diphenylphospholan-1-yl]ethyl]-2, 5-diphenylphospholane; rhodium; tetrafluoroborate. Canonical SMILES: [B-] (F) (F) (F) F. C1CC=CCCC=C1. C1CC (P (C1C2=CC=CC=C2) CCP3C (CCC3C4=CC=CC=C4) C5=CC=CC=C5) C6=CC=CC=C6. [Rh]. Catalog: ACM849950534. | |
| 1,2-diacylglycerol 3-α-glucosyltransferase | The enzyme from the bacterium Acholeplasma laidlawii, which lacks a cell wall, produces the major non-bilayer lipid in the organism. The enzyme from the bacterium Agrobacterium tumefaciens acts under phosphate deprivation, generating glycolipids as surrogates for phospholipids. The enzyme belongs to the GT4 family of configuration-retaining glycosyltransferases. Many diacylglycerols with long-chain acyl groups can act as acceptors. cf. EC 2.4.1.336, monoglucosyldiacylglycerol synthase. Group: Enzymes. Synonyms: mgs (gene name); UDP-glucose:diacylglycerol glucosyltransferase; UDP-glucose:1,2-diacylglycerol glucosyltransferase; uridine diphosphoglucose-diacylglycerol glucosyltransferas. Enzyme Commission Number: EC 2.4.1.337. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2575; 1,2-diacylglycerol 3-α-glucosyltransferase; EC 2.4.1.337; mgs (gene name); UDP-glucose:diacylglycerol glucosyltransferase; UDP-glucose:1,2-diacylglycerol glucosyltransferase; uridine diphosphoglucose-diacylglycerol glucosyltransferase; UDP-glucose-diacylglycerol glucosyltransferase; UDP-glucose:1,2-diacylglycerol 3-D-glucosyltransferase; UDP-glucose:1,2-diacyl-sn-glycerol 3-D-glucosyltransferase; 1,2-diacylglycerol 3-glucosyltransferase (ambiguous). Cat No: EXWM-2575. | |
| 1,2-Dioleoyl-sn-glycerol | ALN29882 is a glycerolipid located on the plasma membrane. It consists of two fatty acid chains covalently linked to a single glycerol molecule by means of an ester bond. 18:1 DG has been used as a source of diacylglycerol in the diacylglycerol O-acyltransferase 1 (DGAT1) assay. It is also used as a substrate in the DGAT-1 enzyme assay to evaluate compounds as potential inhibitors of DGAT-1. Suitable for lipoprotein overlay screening assays with the recombinant protein His-AtROP6. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: sn-1,2-Dioleoylglycerol. CAS No. 24529-88-2. Pack Sizes: 5 mg; 10 mg; 25 mg. Product ID: HY-141572. | |
| 1,3,4,6-Tetra-O-acetyl-2-deoxy-2-N-phthalimido-a-D-glucopyranose | 1,3,4,6-Tetra-O-acetyl-2-deoxy-2-N-phthalimido-a-D-glucopyranose, a chemical compound utilized in the production of glycopeptide antibiotics, demonstrates its functional potential as an acyl donor in the course of synthesizing vancomycin derivatives. Resistant against MRSA and other drug-resistance bacteria, said derivatives showcase their potential to alleviate the issues precipitated by such pathogens. Synonyms: 1,3,4,6-Tetraacetyl-2-deoxy-2-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)-a-D-glucopyranose. CAS No. 31505-44-9. Molecular formula: C22H23NO11. Mole weight: 477.42. | |
| 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide methiodide | 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide methiodide is a water soluble carbodiimide used as an amide coupling reagent and cross-linking agent. 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide methiodide is effective in amide coupling where either the amine or the carboxylic acid is immobilised onto a polymeric solid support, such as core-shell structured nanoaggregates including nanospheres and nanorods. 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide methiodide can be also employed in the binding formation of DNA with N-acylurea derivatives of proteins, such as albumin and transferrin. Group: Biochemicals. Alternative Names: EDC methiodide; EDAC MeI. Grades: Highly Purified. CAS No. 22572-40-3. Pack Sizes: 5g, 10g, 25g, 50g, 100g. Molecular Formula: C8H17N3·CH3I, Molecular Weight: 297.18. US Biological Life Sciences. | Worldwide |
| 1,3-Dipalmitoyl-rac-glycerol | 1,3-Dipalmitoyl-rac-glycerol is a diacylglycerol that contains palmitic acid at the sn-1 and sn-3 positions. It activates protein kinase C α (PKCα) in vitro (Ka = 3.8 μM). 1,3-Dipalmitoyl-rac-glycerol (0.25-2 μM) inhibits apoptosis and production of reactive oxygen species (ROS) and pro-inflammatory mediators induced by oxygen-glucose deprivation and reperfusion (OGD/R) in SH-SY5Y neuroblastoma cells. An acyl acceptor for the unspecific bifunctional wax ester synthase/acyl-CoA:Diacylglycerol acyltransferase. Synonyms: 1,3-Dipalmitin; Dipalmitin; 1,3-Dipalmitoyl-glycerol; Glyceryl 1,3-dipalmitate. Grades: ≥98%. CAS No. 502-52-3. Molecular formula: C35H68O5. Mole weight: 568.91. | |
| 13-hydroxylupanine O-tigloyltransferase | Benzoyl-CoA and, more slowly, pentanoyl-CoA, 3-methylbutanoyl-CoA and butanoyl-CoA can act as acyl donors. Involved in the synthesis of lupanine alkaloids. Group: Enzymes. Synonyms: tigloyl-CoA:13-hydroxylupanine O-tigloyltransferase; 13-hydroxylupanine acyltransferase. Enzyme Commission Number: EC 2.3.1.93. CAS No. 85341-00-0. Storage: Store it at +4 ?C for short term. For long term storage, store it at -20 ?C?-80 ?C. Form: Liquid or lyophilized powder. EXWM-2275; 13-hydroxylupanine O-tigloyltransferase; EC 2.3.1.93; 85341-00-0; tigloyl-CoA:13-hydroxylupanine O-tigloyltransferase; 13-hydroxylupanine acyltransferase. Cat No: EXWM-2275. | |
| 1-(3-Methoxyphenyl)ethanol | 1-(3-Methoxyphenyl)ethanol (Rivastigmine EP Impurity G) is a versatile reactant used in the preparation of 2,3-dihydroimidazo[1,2-a]pyridines as enantioselective acyl transfer catalysts in kinetic resolution of alcohols. Also used in chemoselective preparation of aryl aldehydes/ketones via in situ generated TEMPO-copper(II) diimine catalyzed oxidation of benzylic alcohols in aqueous media. Group: Biochemicals. Grades: Highly Purified. CAS No. 23308-82-9. Pack Sizes: 50mg, 250mg. Molecular Formula: C9H12O2. US Biological Life Sciences. | Worldwide |
| 1,3-O-Bis(triisopropylsilyl) 2-Oleoyl Glycerol-d5 | Protected, labeled 2-Acylglycerol metabolite. Group: Biochemicals. Alternative Names: (9Z)-9-Octadecenoic Acid 2-Triisopropyl silyloxy-1- (triisopropyl silyloxymethyl) ethyl-d5 Ester; 1,3-O-Bis(triisopropylsilyl)-2-monoolein-d5; 1,3-O-Bis(triisopropylsilyl)-2-monooleoylglycerol-d5; 1,3-O-Bis(triisopropylsilyl)-2-oleoylglycerol-d5; 1,3-O-Bis(triisopropylsilyl)-glycerol-d5 1,3-O-Bis(triisopropylsilyl)-2-monooleate; 1,3-O-Bis(triisopropylsilyl)- β-monoolein-d5. Grades: Highly Purified. Pack Sizes: 5mg. US Biological Life Sciences. | Worldwide |
| 14:0 EPC chloride | 14:0 EPC chloride is an acyl cationic lipid that can be used for liposomes applied in drug delivery [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 186492-53-5. Pack Sizes: 10 mg; 25 mg. Product ID: HY-144021. | |
| 14-Pentadecynoic Acid | 14-Pentadecynoic Acid is a reagent in the study of palmitoylation by the hedgehog acyltransferase. Group: Biochemicals. Grades: Highly Purified. CAS No. 212913-84-3. Pack Sizes: 10mg, 25mg. Molecular Formula: C15H26O2, Molecular Weight: 238.37. US Biological Life Sciences. | Worldwide |
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