Find where to buy products from suppliers in the USA, including: distributors, industrial manufacturers in America, bulk supplies and wholesalers of raw ingredients & finished goods.
Search for products or services, then visit the American suppliers website for prices, SDS or more information. You can also view suppliers in Australia, NZ or the UK.
| Product | Description | |
|---|---|---|
| 1, 1-Bis (diphenylphosphino) ferrocene | Commonly used coordination compound in synthesis, readily forms complexes with various metals, i.e. when reacting with the acetonitrile or benzonitrile complexes of PdCl2 it forms (dppf)PdCl2, which is a popular reagent for palladium-catalyzed coupling reactions. Group: Biochemicals. Alternative Names: Cyclopentadienyl diphenyl phosphine; 1, 1'-Ferrocendiylbis (diphenylphosphine); dppf. Grades: Highly Purified. CAS No. 12150-46-8. Pack Sizes: 10g, 25g, 50g, 100g, 250g. Molecular Formula: C??H??FeP?, Molecular Weight: 554.38. US Biological Life Sciences. |  Worldwide |
| 1,1'-Bis(diphenylphosphino)ferrocene Dioxide | 1,1'-Bis(diphenylphosphino)ferrocene Dioxide is a coordination compound used to complex with various metals and form reagents to be used as catalysts in coupling reactions. Group: Iron compound. CAS No. 32660-24-5. Molecular formula: C34H28FeO2P2. Mole weight: 586.38. Catalog: ACM32660245. |  |
| 1,1'-Bis(diphenylphosphino)ferrocene monooxide | 1,1'-Bis(diphenylphosphino)ferrocene monooxide is a coordination compound used to complex with various metals and form reagents to be used as catalysts in coupling reactions. Group: Heterocyclic organic compound. Alternative Names: 1-(Diphenylphosphino)-1'-(diphenylphosphinyl)ferrocene. CAS No. 134537-54-5. Molecular formula: C34H28FeOP2. Mole weight: 570.38. Purity: 0.96. IUPACName: 1-(diphenylphosphino)-1-(diphenyloxophosphoryl)ferrocene. Catalog: ACM134537545. | |
| 1-(2-Mesitylenesulfonyl)-3-nitro-1H-1,2,4-triazole | An efficient coupling reagent in oligonucleotide synthesis by the phosphotriesters approach. Synonyms: MSNT 1-(Mesitylene-2-sulfonyl)-3-nitro-1,2,4-triazole; 1-(mesitylsulfonyl)-3-nitro-1h-1,2,4-triazole; MSNT; 1-(2,4,6-Trimethylphenylsulfonyl)-3-nitro-1,2,4-triazole; 3-nitro-1-(2,4,6-trimethylbenzenesulfonyl)-1H-1,2,4-triazole; Oprea1_756023; KSC491C8B; SCHEMBL216889. Grades: 98 %. CAS No. 74257-00-4. Molecular formula: C11H12N4O4S. Mole weight: 296.30. |  |
| 1-(2-Mesitylenesulfonyl)-3-Nitro-1H-1,2,4-Triazole (MSNT) | An efficient coupling reagent in oligonucleotide synthesis by the phosphotriesters approach. Group: Biochemicals. Alternative Names: MSNT. Grades: Highly Purified. Pack Sizes: 2g. US Biological Life Sciences. | Worldwide |
| 1,2-Phenylene Phosphorochloridite | Highly reactive cyclic phosphitylating reagent which provides fast coupling rates, and hydrolytic cleavage occurs more readily than with acyclic analogs. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10g. US Biological Life Sciences. | Worldwide |
| 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide HCl (EDAC, EDC) | Commonly known as EDAC, EDC or EDCI, this carbodiimide HCl salt is used as a coupling reagent in the synthesis of amides and carboxylic esters. EDAC is highly soluble in water and in most organic solvents, it can be employed in liquid and solid-phase and synthesis. The major advantage of EDCI over other carbodiimides such as DCC and DIC is the ease of purification of the product from the water-soluble urea by-product by washing the crude mixture with water or mild acid and extracting in the organic phase. The main applications of EDAC are in peptide synthesis, Steglich esterification reactions in presence of catalytic DMAP, immunoconjugate synthesis, synthesis of sulfo-NHS esters and coupling of biomolecules onto solid supports. Group: Biochemicals. Alternative Names: EDC.HCl; EDAC. HCl; Water Soluble Carbodiimide; N-Ethyl-N'- (3-dimethylaminopropyl) carbodiimide HCl; 1-Ethyl-3- (3-dimethylaminopropyl) carbodiimide HCl. Grades: Highly Purified. CAS No. 25952-53-8. Pack Sizes: 25g, 50g, 100g, 250g, 500g. Molecular Formula: C8H17N3·HCl, Molecular Weight: 191.7. US Biological Life Sciences. | Worldwide |
| 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 |
| 1,4-Benzenediboronic acid bis(pinacol) ester | Reagent used for Suzuki-Miyaura cross-coupling reactions and polymerizations Reagent used in Prepration of Efficient solar cell photoelectric polymers Field-effect transistors and photovoltaic cells Fluorescent compounds and materials such as Blue OLED devices, Blue Polymeric Light Emitting Diodes, and White LEDs. Uses: Reagent used for suzuki-miyaura cross-coupling reactions and polymerizations reagent used in prepration of efficient solar cell photoelectric polymers field-effect transistors and photovoltaic cells fluorescent compounds and materials such as blue oled devices, blue polymeric light emitting diodes, and white leds. Group: Saltsmall molecule semiconductor building blockssemiconductor blocks. Alternative Names: 1,4-Phenylenebis(4,4,5,5-tetramethyl-1,3,2-dioxaborolane), 1,4-Bis(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)benzene, cyclic bis(tetramethylethylene) ester p-Benzenediboronic acid, 1,4-Benzenediboronic acid dipinacol ester. CAS No. 99770-93-1. Product ID: 4,4,5,5-tetramethyl-2-[4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl]-1,3,2-dioxaborolane. Molecular formula: 330.03. Mole weight: C6H4[B(OH)2]2. CC1 (C)OB (OC1 (C)C)c2ccc (cc2)B3OC (C) (C)C (C) (C)O3. 1S/C18H28B2O4/c1-15 (2)16 (3, 4)22-19 (21-15)13-9-11-14 (12-10-13)20-23-17 (5, 6)18 (7, 8)24-20/h9-12H, 1-8H3. UOJCDDLTVQJPGH-UHFFFAOYSA-N. >98.0%(GC). |  |
| 1-Bromo-2-cyclohexylethane | 1-Bromo-2-cyclohexylethane is a reagent used in the cross-coupling and Grignard reactions. It is used in the synthesis of immunosuppressive agents consisting of 5-phenylalkoxypsoralens as well as agonists for human vitamin-D resistant Rickets. Group: Biochemicals. Alternative Names: (2-Bromoethyl) cyclohexane; (2-Bromoethyl) cyclohexane; 1-Bromo-2-cyclohexylethane; 2-Cyclohexylethyl Bromide; NSC 46808; NSC 6078. Grades: Highly Purified. CAS No. 1647-26-3. Pack Sizes: 2.5g. US Biological Life Sciences. | Worldwide |
| 1-Bromo-2-methoxy-naphthalene | 1-Bromo-2-methoxy-naphthalene is a useful synthetic intermediate. It is used as a reagent to syntheisze a catalyst for highly enantioselective aziridination of styrene derivatives. It can also be used to prepare biaryls or biheterocycles by palladium-catalyzed Ullmann coupling. Group: Biochemicals. Grades: Highly Purified. CAS No. 3401-47-6. Pack Sizes: 5g, 25g. Molecular Formula: C11H9BrO, Molecular Weight: 237.09. US Biological Life Sciences. | Worldwide |
| 1-Methyl-1H-pyrazole-4,5-diamine Sulfate | 1-Methyl-1H-pyrazole-4,5-diamine sulfate is used as a coupling reagent in synthetic hair dye products. Group: Biochemicals. Grades: Highly Purified. CAS No. 20055-01-0. Pack Sizes: 500mg, 5g. Molecular Formula: C4H10N4O4S, Molecular Weight: 210.21. US Biological Life Sciences. | Worldwide |
| 1-O-tert-Butyldimethylsilyl-5-O-DMT-2-O-methyl-D-ribose 3-CE-phosphoramidite | Introducing 1-O-tert-Butyldimethylsilyl-5-O-DMT-2-O-methyl-D-ribose 3-CE-phosphoramidite - a highly specialized biochemical reagent utilized in synthesizing oligonucleotides for diverse biomedical research applications. This unique compound is widely recognized for its capability to incorporate modified nucleosides into DNA or RNA molecules with remarkable precision and efficiency, thereby enhancing the specificity and stability of oligonucleotides engineered to target lethal diseases like cancer. Remarkably pure and compatible with various coupling agents, this revolutionary reagent offers immense potential in advancing biomedical research. Molecular formula: C42H61N2O8PSi. Mole weight: 781.00. | |
| (1R,2S,4R)-4-Amino-2-hydroxy-cyclopentanemethanol Hydrochloride | (1R,2S,4R)-4-Amino-2-hydroxy-cyclopentanemethanol Hydrochloride can be used as a reagent/reactant for stereoselective synthesis and antiviral activity of carbocyclic nucleoside analog of pentyl phenyl furopyrimidine deoxyribose via stereoselective hydroboration, heterocyclization and Sonogashira coupling from Vince lactam (1). (1R,2S,4R)-4-Amino-2-hydroxy-cyclopentanemethanol Hydrochloride can also be obtained from (1R)-(-)-2-Azabicyclo[2.2.1]hept-5-en-3-one (A795205) which is an Abacavir intermediate used in the synthesis of carbocyclic sugar amines, carbanucleosides, and carbocyclic dinucleotide analogues (2). Group: Biochemicals. Grades: Highly Purified. CAS No. 155750-92-8. Pack Sizes: 100mg, 250mg. Molecular Formula: C6H13NO2 HCl, Molecular Weight: 131.173645999999. US Biological Life Sciences. | Worldwide |
| 2-(1-Oxy-pyridin-2-yl)-1,1,3,3-tetramethylisothiouronium tetrafluoroborate | A new reagent for peptide coupling and amidation reactions. Synonyms: TOTTS-(1-Oxo-2-pyridyl)-thio-N,N,N',N'-tetramethyluronium tetrafluoroborate; TOTT S-(1-Oxo-2-pyridyl)-thio-N,N,N',N'-tetramethyluronium tetrafluoroborate; N,N,N',N'-Tetramethyl-S-(1-oxido-2-pyridyl)thiuronium tetrafluoroborate; N,N,N inverted exclamation marka,N inverted exclamation marka-Tetramethyl-S-(1-oxido-2-pyridyl)thiuronium tetrafluoroborate; S-(2-Pyridyl)-N,N,N inverted exclamation marka,N inverted exclamation marka-tetramethylthiuronium N-oxide tetrafluoroborate; TOTT. Grades: ≥ 99% (HPLC). CAS No. 255825-38-8. Molecular formula: C10H16BF4N3OS. Mole weight: 313.12. | |
| 2,2':5',2''-TERTHIOPHENE | 2,2':5',2''-Terthiophene (TTh) may be prepared by nickel catalysed coupling reaction of grignard's reagent derived from 2-bromothiophene and magnesium. It generates singlet oxygen. In nature, it is found in the floral extract of Tagetes minuta and Echinops grijisii. It is known to be toxic to mosquitoes. It also exihibits antifungal activity. 2,2':5',2''-Terthiophene (3T) is a tri-thiophene based low band conductive polymer that is prepared by reacting 2,5-dibromothiophene and thienylmagnesium bromide in the presence of nickel catalyst. Uses: 3t can be combined with 3,4-ethylenedioxythiophene (edot) in a tetrabutylammonium perchlorate solution for use as an electrochromic copolymer for a wide range of s like photovoltaics and polymer light emitting diodes (leds). it can also be used to form metal-organic based thin films with metals like aluminum, silver, and calcium which can potentially be used for optoelectronics based s. electroche. Group: other electronic materials synthetic tools and reagents. Alternative Names: 2,5-Di(thien-2-yl)thiophene. CAS No. 1081-34-1. Pack Sizes: Packaging 1 g in glass bottle. Product ID: 2,5-Dithiophen-2-ylthiophene. Molecular formula: 248.4. Mole weight: C12H8S3. C1=CSC(=C1)C2=CC=C(S2)C3=CC=CS3. InChI=1S/C12H8S3/c1-3-9 (13-7-1)11-5-6-12 (15-11)10-4-2-8-14-10/h1-8H. KXSFECAJUBPPFE-UHFFFAOYSA-N. 95%+. | |
| 2,2-Dipyridyl disulfide | 2,2-Dipyridyl disulfide is a useful reagent for the determination of sulfhydryl groups. 2,2-Dipyridyl disulfide is a common reagent in peptide chemistry, often used in oxidation - reduction condensations to form peptide bonds or in coupling reactions to form disulfide-linked heterodimers [1]. Uses: Scientific research. Group: Signaling pathways. CAS No. 2127-3-9. Pack Sizes: 10 mM * 1 mL; 5 g. Product ID: HY-Y1666. |  |
| 2,3,4,6-Tetra-O-benzoyl-D-galactopyranosyl trichloroacetimidate | 2,3,4,6-Tetra-O-benzoyl-D-galactopyranosyl trichloroacetimidate plays a pivotal role in glycosylation reactions as an effective coupling reagent, contributing to the synthesis of diverse glycosides and glycoconjugates. By utilizing its potential in the formation of oligosaccharides containing galactosyl or other carbohydrate sequences, promising therapeutic agents can be developed, targeting diseases such as cancer and inflammation with a high degree of specificity and efficacy. Molecular formula: C36H28Cl3NO10. Mole weight: 740.97. | |
| 2,3-Dimethylbiphenyl | 2,3-Dimethylbiphenyl acts as a reagent in the preparation of carbene complexes that functions as catalyst for Suzuki coupling reactions. It also functions as an intermediate for organic synthesis. Group: Biochemicals. Grades: Highly Purified. CAS No. 3864-18-4. Pack Sizes: 100mg, 250mg. Molecular Formula: C14H14, Molecular Weight: 182.26. US Biological Life Sciences. | Worldwide |
| 2,4,4,5,5-Pentamethyl-1,3,2-dioxaborolane | 2,4,4,5,5-Pentamethyl-1,3,2-dioxaborolane is a coupling reagent used in the stereoselective synthesis of spirocyclic ketones. Group: Biochemicals. Grades: Highly Purified. CAS No. 94242-85-0. Pack Sizes: 500mg, 1g. Molecular Formula: C7H15BO2, Molecular Weight: 142. US Biological Life Sciences. | Worldwide |
| 2,4,6-Trimethoxyboroxin | 2,4,6-Trimethoxyboroxin is a coupling reagent used in the preparation of electrocatalysis paradigms for the protection of cathode materials in high-voltage lithium ion batteries. Group: Biochemicals. Grades: Highly Purified. CAS No. 102-24-9. Pack Sizes: 5g, 10g. Molecular Formula: C3H9B3O6, Molecular Weight: 173.53. US Biological Life Sciences. | Worldwide |
| 2,4-Dimethylbiphenyl | 2,4-Dimethylbiphenyl is a reagent used in the preparation of palladium(II) complexes with chelating biscarbene ligands for Suzuki-Miyaura cross-coupling reaction. Group: Biochemicals. Grades: Highly Purified. CAS No. 4433-10-7. Pack Sizes: 50mg, 100mg. Molecular Formula: C14H14, Molecular Weight: 182.26. US Biological Life Sciences. | Worldwide |
| 2,5-Bis(trimethylstannyl)-thieno[3,2-b]thiophene | 2,5-Bis(trimethylstannyl)-thieno[3,2-b]thiophene is a conducting polymer that can be used in the formation of the hole transporting material (HTM) with improved charge mobility. It is a majorly utilized as a copolymer in the polymerization of new thieno(3,2-b)thiophene based polymers. Uses: 2,5-bis(trimethylstannyl)-thieno[3,2-b]thiophene can be used as a copolymer in the synthesis of thiophene based materials for the fabrication of organic electronic devices such as organic field effect transistors (ofets), organic thin film transistors(otfts) and organic photovoltaic cells (opvs). 2,5-bis(trimethylstannyl)-thieno[3,2-b]thiophene is a synthetic intermediate, which can be used in the synthesis of polythiophenes based fluorinated polymers for the optoelectronic s. it can also be used in the synthesis of pdbt-co-tt via still coupling polymerization for the fabrication of organic thin film transistors (otfts)and photovoltaic devices. Group: Synthetic tools and reagents. Pack Sizes: Packaging 1, 5 g in glass bottle. Product ID: trimethyl-(5-trimethylstannylthieno[3,2-b]thiophen-2-yl)stannane. Molecular formula: 465.84. Mole weight: C12H20S2Sn2. C[Sn](C)(C)c1cc2sc(cc2s1)[Sn](C)(C)C. 1S/C6H2S2. 6CH3. 2Sn/c1-3-7-6-2-4-8-5(1)6; ; ; ; ; ; ; ; /h1-2H; 6*1H3;. HDZULVYGCRXVNQ-UHFFFAOYSA-N. ≥ 97%. | |
| 2,5-Dibromo-3,4-dinitrothiophene | 2,5-Dibromo-3,4-dinitrothiophene. Uses: This monomer is useful in the pd catalyzed stille coupling to make conjugated thiophene oligomers or co-oligomers. the corresponding amine(s) can be obtained by subsequent reduction. Group: other electronic materials synthetic tools and reagents. Alternative Names: 2,5-DIBROMO-3,4-DINITROTHIOPHENE; AKOS 92299; 2,5-Dibromo-3,4-dinitrthiphene; 2,5-DIBROMO-3,4-DINITROTHIOPHENE 98+%; 2,5-DibroMo-3,4-dinitrothiophene98%; NSC 84661; DibroMo-3,4-dinitrothio; 2,5-Dibromo-3,4-dinitrothiophene,95%. CAS No. 52431-30-8. Pack Sizes: Packaging 1, 5 g in glass bottle. Product ID: 2,5-dibromo-3,4-dinitrothiophene. Molecular formula: 331.93. Mole weight: C4Br2N2O4S. [O-][N+] (=O)c1c (Br)sc (Br)c1[N+] ([O-])=O. 1S/C4Br2N2O4S/c5-3-1 (7 (9)10)2 (8 (11)12)4 (6)13-3. AHGHPBPARMANQD-UHFFFAOYSA-N. 98%. | |
| 2,5-Dimethyl-1,1'-biphenyl | 2,5-Dimethyl-1,1'-biphenyl is a useful reagent for organic synthesis. It is used in the preparation of orthopalladated phosphorus ylide complexes and palladium nanoparticles as catalyst for Suzuki coupling reactions. Group: Biochemicals. Grades: Highly Purified. CAS No. 7372-85-2. Pack Sizes: 100mg, 500mg. Molecular Formula: C14H14, Molecular Weight: 182.26. US Biological Life Sciences. | Worldwide |
| 2-(5-Norbornen-2,3-dicarboximido)-1,1,3,3-tetramethyluronium tetrafluoroborate | Coupling reagent for peptide synthesis giving low racemization. Synonyms: TNTUO-(5-Norbornene-2,3-dicarboximido)-N,N,N',N'-tetramethyluronium tetrafluoroborate; TNTU; 2-(1,3-Dioxo-3a,4,7,7a-tetrahydro-1H-4,7-methanoisoindol-2(3H)-yl)-1,1,3,3-tetramethyluronium tetrafluoroborate; 2-(endo-5-norbornene-2,3-dicarboxylimide)- -1,1,3,3-tetramethyluroniumtetrafluoroborate; Methanaminium, N-[(dimethylamino)[(1,3,3a,4,7,7a-hexahydro-1,3-dioxo-4,7-methano-2H-isoindol-2-yl)oxy]methylene]-N-methyl-, tetrafluoroborate(1-) (1:1); O-(5-Norbornene-2,3-dicarboximido)-N,N,N',N'-tetramethyluronium tetrafluoroborate; SCHEMBL360038. Grades: ≥ 99% (HPLC). CAS No. 125700-73-4. Molecular formula: C14H20BF4N3O3. Mole weight: 365.13. | |
| 2,6-Dichloro-4-pyridinemethanol | 2,6-Dichloro-4-pyridinemethanol is a reagent in the preparation of functionalized compounds such as bipyridines and terpyridines via Stille-type cross coupling. Also used in the preparation of fluorescent chemosensors. Group: Biochemicals. Grades: Highly Purified. CAS No. 101990-69-6. Pack Sizes: 1g, 5g. Molecular Formula: C6H5Cl2NO, Molecular Weight: 178.02. US Biological Life Sciences. | Worldwide |
| 2,6-Dimethylbiphenyl | 2,6-Dimethylbiphenyl acts as a reagent in the preparation of palladium catalyst for Suzuki-Miyaura cross-coupling reactions. Group: Biochemicals. Grades: Highly Purified. CAS No. 3976-34-9. Pack Sizes: 50mg, 100mg. Molecular Formula: C14H14, Molecular Weight: 182.26. US Biological Life Sciences. | Worldwide |
| 2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-a-D-galactopyranosyl-(N-Fmoc)-L-serine pentafluorophenyl ester | 2-Acetamido-3,4,6-tri-O-acetyl-2-deoxy-a-D-galactopyranosyl-(N-Fmoc)-L-serine pentafluorophenyl ester is an essential and sophisticated chemical reagent in peptide synthesis. It introduces considerable burstiness and perplexity in developing therapeutic peptides, which characteristically treat cancer and infectious diseases. Its adoption in peptide coupling reactions is a crucial implementation for the progression of scientific and medical research. CAS No. 137816-29-6. Molecular formula: C38F5H35N2O13. Mole weight: 822.69. | |
| 2-Amino-N,N,3-trimethyl-butanamide | 2-Amino-N,N,3-trimethyl-butanamide is a reagent used in the preparation of dipeptides under abiotic conditions and stereochemistry preference in competitive peptide coupling reactions. Group: Biochemicals. Grades: Highly Purified. CAS No. 230643-41-1. Pack Sizes: 250mg, 2.5g. Molecular Formula: C7H16N2O, Molecular Weight: 144.21. US Biological Life Sciences. | Worldwide |
| 2-Amino-N,N,3-trimethyl-butanamide-d6 | 2-Amino-N,N,3-trimethyl-butanamide-d6 is the isotope analog of 2-Amino-N,N,3-trimethyl-butanamide. 2-Amino-N,N,3-trimethyl-butanamide is a reagent used in the preparation of dipeptides under abiotic conditions and stereochemistry preference in competitive peptide coupling reactions. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 5mg, 50mg. Molecular Formula: C7H10D6N2O, Molecular Weight: 150.25. US Biological Life Sciences. | Worldwide |
| 2-?Bromo-?1,?3,?2-?benzodioxaborole | 2-?Bromo-?1,?3,?2-?benzodioxaborole is a coupling reagent used in the synthesis of ustiloxin natural products used for their antimitotic activity. Group: Biochemicals. Grades: Highly Purified. CAS No. 51901-85-0. Pack Sizes: 500mg, 1g. Molecular Formula: C6H4BBrO2, Molecular Weight: 198.81. US Biological Life Sciences. | Worldwide |
| 2-?Chloro-?1,?3,?2-?benzodioxaborole | 2-?Chloro-?1,?3,?2-?benzodioxaborole is a coupling reagent used in the synthesis of alkenyl boronic esters, obtained from unfunctionalized alkenes. Group: Biochemicals. Grades: Highly Purified. CAS No. 55718-76-8. Pack Sizes: 100mg, 500mg. Molecular Formula: C6H4BClO2, Molecular Weight: 154.36. US Biological Life Sciences. | Worldwide |
| 2-Chloro-1,3,2-benzodioxaphosphorin-4-one | Highly reactive cyclic phosphitylating reagent which provides fast coupling rates, and hydrolytic cleavage occurs more readily than with acyclic analogs. Group: Heterocyclic organic compound. Alternative Names: C7H4ClO3P; AB1011462; 2-Chloro-2H,4H-1,3,2-benzodioxaphosphinin-4-one; 4H-1,3,2-Benzodioxaphosphorin-4-one, 2-chloro-; C-09782; OR3651T; NSC-40209; 5381-99-7; Van Boom's Reagent; 2-chloro-4 H-1,3,2-benzodioxaphosphorin-4-one. CAS No. 5381-99-7. Molecular formula: C7H4ClO3P. Mole weight: 202.53g/mol. IUPACName: 2-chloro-1,3,2-benzodioxaphosphinin-4-one. Canonical SMILES: C1=CC=C2C(=C1)C(=O)OP(O2)Cl. Catalog: ACM5381997. | |
| 2-Chloro-1,3,2-dioxaphospholane | Highly reactive cyclic phosphitylating reagent which provides fast coupling rates, and hydrolytic cleavage occurs more readily than with acyclic analogs. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10g. US Biological Life Sciences. | Worldwide |
| 2-Chloro-1,3,2-dioxaphospholane | Highly reactive cyclic phosphitylating reagent which provides fast coupling rates, and hydrolytic cleavage occurs more readily than with acyclic analogs. Group: Heterocyclic organic compound. Alternative Names: EINECS 212-499-4; 2-Chloro-1,3,2-dioxaphospholane; Ethylene chlorophosphite; AC1Q3VIZ; SC-09222; CTK5E9529; AB1011463; 42280-EP2311829A1; V2040; Ethylene phosphorochloridite(2-chloro-1,3,2-dioxap. CAS No. 822-39-9. Molecular formula: C2H4ClO2P. Mole weight: 126.476g/mol. IUPACName: 2-chloro-1,3,2-dioxaphospholane. Canonical SMILES: C1COP(O1)Cl. ECNumber: 212-499-4. Catalog: ACM822399. | |
| 2-Chloro-4H-1,2,3-benzodioxaphosphorin-4-one | Highly reactive cyclic phosphitylating reagent which provides fast coupling rates, and hydrolytic cleavage occurs more readily than with acyclic analogs. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10g. US Biological Life Sciences. | Worldwide |
| 2-Chlorobutyric Acid (~90%) | 2-Chlorobutyric Acid is used in the preparation of α-chloro esters and their enantioselective coupling with aryl Grignard reagents in the presence of Fe(acac)3 and a nonracemic benzenediphosphine to give α-alkylarylacetates. Group: Biochemicals. Grades: Highly Purified. CAS No. 4170-24-5. Pack Sizes: 250mg, 1g. Molecular Formula: C4H7ClO2, Molecular Weight: 122.55. US Biological Life Sciences. | Worldwide |
| 2-?(Chloromethyl)?allyl-?trimethylsilane | 2-?(Chloromethyl)?allyl-?trimethylsilane is one of the reagents to synthesize Leucasandrolide A Macrolide (I) via Mukaiyama aldol coupling. Group: Biochemicals. Grades: Highly Purified. CAS No. 18388-03-9. Pack Sizes: 250mg, 500mg. Molecular Formula: C7H15ClSi, Molecular Weight: 162.729999999999. US Biological Life Sciences. | Worldwide |
| 2-Dicyclohexylphosphino-2',4',6'-triisopropylbiphenyl | Exceptional ligands for Pd-catalyzed amination and amidation of aryl sulfonates. Ligand used for the Pd-catalyzed Suzuki-Miyaura coupling reaction and carbonyl enolate coupling. Ligand used for the chemoselective amination of aryl chlorides. Ligand used for the Pd-catalyzed borylation of aryl chlorides, for the formation of trifluoroborates. Ligand used for the Pd-catalyzed amination of vinyl halides and triflates. Ligand used for the Pd-catalyzed three-component synthesis of indoles. Ligand used for the Pt-catalyzed regioselective hydrosilylation of functionalized terminal arylalkynes. Ligand used for the Pd-catalyzed synthesis of carbazoles. Ligand used for the Pd-catalyzed Suzuki-Miyaura coupling of aryl chloride and NHC-boranes. Ligand used for the direct arylation of picoline N-oxide. Ligand used for the Negishi coupling of 2-heterocyclic organozinc reagents. Catalyst for a phosphine-catalyzed Heine reaction. Ligand used for the palladium-catalyzed oxidative coupling of indoles and heteroarenes. Ligand used for the silver-catalyzed hydrogenation of aldehydes. Ligand used for the palladium-catalyzed cyanation of heterycyclic halides. Group: Organic phosphine compounds. Alternative Names: Dicyclohexyl(2', 4', 6'-Triisopropylbiphenyl-2-Yl)Phosphine. CAS No. 564483-18-7. Molecular formula: C33H49P. Mole weight: 476.72. Appearance: Solid. Purity: 0.98. IUPACName: dicyclohexyl-[2-[2,4, | |
| 2-Dicyclohexylphosphino-2',6'-dimethoxybiphenyl | Ligand/palladium catalyst for general Suzuki-Miyaura cross-coupling reactions. Ligand/palladium catalyst for the Suzuki-Miyaura coupling of aryltrifluoroborates with aryl chlorides. Ligand/palladium catalyst for the Suzuki-Miyaura reaction of heteroaryl halides and heteroaryl boronic acids and esters. Ligand/palladium catalyst for the Kumada-Corriu cross-coupling reaction. Ligand/palladium catalyst for the borylation of aryl halides with pinacol borane. Suzuki couplings involving amino acids. Synthesis of biaryl derivatives of 4-hydroxyphenyl glycine, tyrosine and tryptophan. Synthesis of substituted adamantylzinc reagents using Mg-insertion in the presence of zinc chloride. Highly efficient catalyst for the palladium-catalyzed Suzuki-Miyura reaction of heteroaryl halides and heteroaryl boronic acids and esters. Group: Organic phosphine compounds. Alternative Names: S-PHOS. CAS No. 657408-07-6. Molecular formula: C26H35O2P. Mole weight: 410.53. Appearance: Solid. Purity: 0.98. IUPACName: dicyclohexyl-[2-(2,6-dimethoxyphenyl)phenyl]phosphane. Canonical SMILES: COC1=C (C (=CC=C1)OC)C2=CC=CC=C2P (C3CCCCC3)C4CCCCC4. Catalog: ACM657408076-1. | |
| 2-(Di-tert-butylphosphino)dimethylaminobenzene | Ligand for the Copper-Catalyzed Suzuki-Miyaura Coupling of Arylboronate Esters and Aryl Iodides Ligand for the Copper-Catalyzed Coupling of Triaryl- and Trialkylindium reagents with Aryl Iodides and Bromides. Group: Other phosphine ligands. CAS No. 415941-58-1. Mole weight: 265.37. Catalog: ACM415941581. | |
| (2E)-2,4-Pentadienoic Acid Methyl Ester | (2E)-2,4-Pentadienoic Acid Methyl Ester is the methyl ester derivative of (2E)-2,4-Pentadienoic Acid (P268350) and is used as a reagent in the synthesis of opp-Dibenzoporphyrins as light-harvesters for Dye-Sensitized Solar Cells (DSSCs). Also used as a reagent in the preparation of allyl chlorides and allylboronates as substrates for stereoselective palladium-catalyzed allyl-allyl cross-coupling. Group: Biochemicals. Grades: Highly Purified. CAS No. 2409-87-2. Pack Sizes: 250mg, 2.5g. Molecular Formula: C6H8O2, Molecular Weight: 112.13. US Biological Life Sciences. | Worldwide |
| (2E)-2,4-Pentadienoic Acid Methyl Ester-d3 | (2E)-2,4-Pentadienoic Acid Methyl Ester-d3 is the isotope labelled analog of (2E)-2,4-Pentadienoic Acid Methyl Ester (P268360); the methyl ester derivative of (2E)-2,4-Pentadienoic Acid (P268350) used as a reagent in the synthesis of opp-Dibenzoporphyrins as light-harvesters for Dye-Sensitized Solar Cells (DSSCs). Also used as a reagent in the preparation of allyl chlorides and allylboronates as substrates for stereoselective palladium-catalyzed allyl-allyl cross-coupling. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 10mg, 100mg. Molecular Formula: C6H5D3O2, Molecular Weight: 115.15. US Biological Life Sciences. | Worldwide |
| (2E)-3-(2-Chlorophenyl)-2-butenoic Acid Methyl Ester | (2E)-3-(2-Chlorophenyl)-2-butenoic Acid Methyl Ester is a reagent used as a cross-coupling partner in the synthesis of pharmaceutical agents. Group: Biochemicals. Grades: Highly Purified. CAS No. 1029612-67-6. Pack Sizes: 100mg, 250mg. Molecular Formula: C11H11ClO2, Molecular Weight: 210.66. US Biological Life Sciences. | Worldwide |
| 2-?Isopropoxy-?4,?4,?6-?trimethyl-?1,?3,?2-?dioxaborinane | 2-?Isopropoxy-?4,?4,?6-?trimethyl-?1,?3,?2-?dioxaborinane is a coupling reagent also used in palladium-catalyzed cross coupling reactions. Group: Biochemicals. Grades: Highly Purified. CAS No. 61676-61-7. Pack Sizes: 250mg, 1g. Molecular Formula: C9H19BO3, Molecular Weight: 186.06. US Biological Life Sciences. | Worldwide |
| 2-?Methoxypyridine-?4-?boronic Acid | 2-?Methoxypyridine-?4-?boronic Acid is a coupling reagent used in the synthesis of effacacious pyrrolopyridazines used as JAK1/3 inhibitors. Group: Biochemicals. Grades: Highly Purified. CAS No. 762262-09-9. Pack Sizes: 500mg, 1g. Molecular Formula: C6H8BNO3, Molecular Weight: 152.94. US Biological Life Sciences. | Worldwide |
| 2'-O-tert-Butyldimethylsilyl-5'-O-DMT-5-methyluridine 3'-CE phosphoramidite | 2'-O-tert-Butyldimethylsilyl-5'-O-DMT-5-methyluridine 3'-CE phosphoramidite, a reagent of paramount importance in RNA synthesis, is employed to facilitate the coupling of uridine derivatives in RNA chain assembly. Researchers rely on this product to investigate RNA structure and function and bolster the development of RNA-based therapies. With its protected phosphoramidite derivative of uridine, this reagent overcomes key challenges in RNA molecule construction and offers a valuable tool for pushing the frontiers of RNA research. Synonyms: 5'-DMT-5-methyluridine-2'-O-TBDMS-3'-CE phosphoramidite. Molecular formula: C46H63N4O9PSi. Mole weight: 875.07. | |
| 2-Oxazolone | 2-Oxazolone is a very useful and versatile tool for synthetic organic chemist. Its derivatives can be used as activating groups in coupling reactions and as efficient and reliable chiral auxiliaries. 2-Oxazolone is also used as a reagent in the synthesis of (±)-8α-hydroxystreptazolone. Group: Biochemicals. Grades: Highly Purified. CAS No. 27584-70-9. Pack Sizes: 100mg, 1g. Molecular Formula: C3H3NO2, Molecular Weight: 85.06. US Biological Life Sciences. | Worldwide |
| 2-Pyridineboronic Acid | 2-Pyridineboronic Acid is used in organic synthesis as a reagent in Suzuki cross-coupling reactions, for example in the synthesis of aryl- and heteroaryl-substituted 3-benzyloxyisothiazoles and novel fluorescent 3-aryl- and 3-methyl-7-aryl-[1,2,3]triazolo[1,5-a]pyridines. Group: Biochemicals. Grades: Highly Purified. CAS No. 197958-29-5. Pack Sizes: 100mg, 250mg. Molecular Formula: C5H6BNO2, Molecular Weight: 122.92. US Biological Life Sciences. | Worldwide |
| 2-Thienylboronic Acid | 2-Thienylboronic Acid is a reagent used for palladium-catalyzed Suzuki-Miyaura cross-couplings. It is also used in preparation of photophysical properties of oxygen-containing polycyclic aromatic triptycenes. Group: Biochemicals. Grades: Highly Purified. CAS No. 6165-68-0. Pack Sizes: 1g, 5g. Molecular Formula: C4H5BO2S, Molecular Weight: 127.96. US Biological Life Sciences. | Worldwide |
| 2-Vinyl-4,4,5,5-tetramethyl-1,3,2-dioxaoborolane | 2-Vinyl-4,4,5,5-tetramethyl-1,3,2-dioxaoborolane is a very useful reagent. It can be used for Suzuki-Miyaura coupling reactions, asymmetric Birch reductive alkylation, stereoselective Cu-catalyzed γ-selective and stereospecific coupling and so on. Group: Biochemicals. Grades: Highly Purified. CAS No. 75927-49-0. Pack Sizes: 1g, 5g. Molecular Formula: C8H15BO2, Molecular Weight: 154.01. US Biological Life Sciences. | Worldwide |
| 3- (4-Methoxyphenyl) benzaldehyde | 3- (4-Methoxyphenyl) benzaldehyde is a reagent used in the preparation of pyridine-pyrazole N-N ligand, an effective catalyst for Suzuki coupling reactions. Group: Biochemicals. Grades: Highly Purified. CAS No. 118350-17-7. Pack Sizes: 250mg, 1g. Molecular Formula: C14H12O2, Molecular Weight: 212.24. US Biological Life Sciences. | Worldwide |
| 3-Amino-3-methylbutanoic Acid, 90% | 3-Amino-3-methylbutanoic Acid acts as a reagent in the preparation of arylsulfonyl methylbutanamides of cycloalkylamines, particularly adamantylamines, as selective inhibitors of human and murine 11 β-hydroxysteroid dehydrogenase type 1. Synthesis of acetylcholine and carbamoylcholine analogs as a functionally selective α4 β2 nicotinic acetylcholine receptor agonist. Phenamide preparation by coupling reaction. Group: Biochemicals. Grades: Highly Purified. CAS No. 625-05-8. Pack Sizes: 250mg, 1g. Molecular Formula: C5H11NO2. US Biological Life Sciences. | Worldwide |
| 3-Bromo-4-fluoro-5-nitrobenzoic Acid | 3-Bromo-4-fluoro-5-nitrobenzoic Acid is a derivative of m-Nitrobenzoic Acid (N494700), a reagent used in the coupling of allyl acetate to allylic, aliphatic and benzylic alcohols. Group: Biochemicals. Grades: Highly Purified. CAS No. 1290117-21-3. Pack Sizes: 250mg, 500mg. Molecular Formula: C7H3BrFNO4, Molecular Weight: 264.01. US Biological Life Sciences. | Worldwide |
| 3-(Diethoxyphosphoryloxy)-1,2,3-benzotriazin-4(3H)-one | 3-(Diethoxyphosphoryloxy)-1,2,3-benzotriazin-4(3H)-one is a peptide coupling reagent used in peptide synthesis. It shows remarkable resistance to racemization. Synonyms: Diethyl 3,4-Dihydro-4-oxo-1,2,3-benzotriazin-3-yl Phosphate; diethyl (4-oxo-1,2,3-benzotriazin-3-yl) phosphate; Diethyl (4-oxobenzo[d][1,2,3]triazin-3(4H)-yl) phosphate; 3-(diethoxyphosphoryloxy)-3h-benzo[d][1,2,3]triazin-4-one; DEPBT. Grades: 95 %. CAS No. 165534-43-0. Molecular formula: C11H14N3O5P. Mole weight: 299.22. | |
| 3-(Ethylthio)-butanoic Acid | 3-(Ethylthio)-butanoic Acid is a reagent in the synthesis of amide using polyer-bound EDC (1-ethyl-3- (3-dimethylaminopropyl) carbodiimide) as coupling reagent. Group: Biochemicals. Grades: Highly Purified. CAS No. 89534-40-7. Pack Sizes: 100mg, 1g. Molecular Formula: C6H12O2S, Molecular Weight: 148.22. US Biological Life Sciences. | Worldwide |
| 3-Hexylthiophene-2-boronic acid pinacol ester | 3-Hexylthiophene-2-boronic acid pinacol ester. Uses: Reagent used for suzuki-miyaura cross-coupling reactions p-type/n-type switching of ambipolar bithiazole-benzothiadiazole-based polymers in solar cells hierarchical self-assembly of semiconductor functionalized peptide a-helixes and optoelectronic properties reagent used in preparation of photovoltaic materials, polymers, and thiophene-based compounds with photophysical, electrochemical, and fluorescent properties polymer solar cells for low band gap poly(1,4-arylene-2,5-thienylene)s with benzothiadiazole units dithienothiophene-based dyes for dye-sensitized solar cells. Group: Saltsynthetic tools and reagents. Alternative Names: 2-(3-Hexyl-2-thienyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane, 3-Hexyl-2-thienylboronic acid. CAS No. 850881-09-3. Pack Sizes: 1, 5 g in glass bottle. Product ID: 2-(3-hexylthiophen-2-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane. Molecular formula: 294.26. Mole weight: C16H27BO2S. CCCCCCc1ccsc1B2OC(C)(C)C(C)(C)O2. 1S / C16H27BO2S / c1-6-7-8-9-10-13-11-12-20-14 (13) 17-18-15 (2, 3) 16 (4, 5) 19-17 / h11-12H, 6-10H2, 1-5H3, XCXAUPBHQCCWCI-UHFFFAOYSA-N. XCXAUPBHQCCWCI-UHFFFAOYSA-N. | |
| (3-Hydroxy-3H-1,2,3-triazolo[4,5-b]pyridinato-O)tri-1-pyrrolidinylphosphonium hexafluorophosphate | PyAOP is a phosphonium salt used as a coupling reagent in Solid-phase peptide synthesis, without undergoing side reactions with the amino terminus. PyAOP is a derivative of HOAt. Synonyms: PyAOP; (7-AZABENZOTRIAZOL-1-YLOXY)TRIPYRROLIDINO-PHOSPHONIUM HEXAFLUOROPHOSPHATE; 7-AZABENZOTRIAZOL-1-YLOXY-TRIS-(PYRROLIDINO)PHOSPHONIUM HEXAFLUOROPHOSPHATE; (7-AZABENZOTRIAZOLE-1-YLOXY)TRIPYRROLIDINOPHOSPHONIUM HEXAFLUOROPHOSPHATE; PYAOP; ((3H-[1,2,3]Triazolo[4,5-b]pyridin-3-yl)oxy)tri(pyrrolidin-1-yl)phosphonium hexafluorophosphate; (7-Azabenzotriazol-1-yloxy)tripyrrolidinophosphonium hexafluorophosphate; (T-4)?-[3-(hydroxy-κO)?-3H-1,?2,?3-triazolo[4,?5-b]?pyridinato]?tri-1-pyrrolidinyl-Phosphorus(1+)? hexafluorophosphate(?1-); tri-1-pyrrolidinyl(3H-1,2,3-triazolo[4,5-b]pyridin-3-yloxy)-Phosphonium hexafluorophosphate(1-). Grades: 98%. CAS No. 156311-83-0. Molecular formula: C17H27N7OP?PF6. Mole weight: 521.38. | |
| 3-Methyl-2-benzothiazolinone Hydrazone Hydrochloride Hydrate | 3-Methyl-2-benzothiazolinone Hydrazone Hydrochloride Hydrate is a chromegenic reagent for the determination of benzodiazepines, cholesterol, and enzyme activity. 3-Methyl-2-benzothiazolinone Hydrazone Hydrochloride Hydrate is used as an electrophilic coupling reagent used in the spectrophotometric determination of chloramine-B (CAB) and other residual chlorine content in various environmental water samples. Group: Biochemicals. Alternative Names: 3-Methyl-2(3H)-benzothiazolone Hydrazone Monohydrochloride Hydrate; MBTH Hydrochloride Hydrate. Grades: Highly Purified. CAS No. 149022-15-1,14448-67-0,4338-98-1. Pack Sizes: 5g, 10g, 25g. Molecular Formula: C?H??ClN?S xH?O, Molecular Weight: 215.7. US Biological Life Sciences. | Worldwide |
| 3-(Trimethoxysilyl)propyl methacrylate | 3-(Trimethoxysilyl)propyl methacrylate ([3- (Methacryloyloxy) propyl]trimethoxysilane) is a silane coupling agent that can be used to modify TiO 2 nanoparticles. 3-(Trimethoxysilyl)propyl methacrylate is a biomaterial or organic compound that can be used for life science research [1]. Uses: Scientific research. Group: Biochemical assay reagents. Alternative Names: [3- (Methacryloyloxy) propyl]trimethoxysilane. CAS No. 2530-85-0. Pack Sizes: 25 g; 100 g. Product ID: HY-W105426. | |
| 4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride | 4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride, also known as DMTMM, is an alcohol and water-soluble coupling reagent used to synthesise amides and esters in a one-step procedure. DMTMM is selective, achieves good yields and can be easily removed under reduced pressure from the reaction mixture. DMTMM finds application in the activation of carboxyl polysaccharides to make glucans, in the functionalisation of poly(acrylic acid) and poly(methacrylic acid) with amines via amide bonds, to make glycoconjugates and for coupling propylamine and butylamine to hyaluronic acid. Group: Biochemicals. Alternative Names: 4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium Chloride; DMTMM; MMTM. Grades: Highly Purified. CAS No. 3945-69-5. Pack Sizes: 10g, 25g, 50g, 100g. Molecular Formula: C??H??ClN?O?, Molecular Weight: 276.72. US Biological Life Sciences. | Worldwide |
| 4-(4,6-Dimethoxy-1,3,5-triazin-2-yl)-4-methylmorpholinium chloride | DMTMM, a conjugating agent that efficiently conjugat PnPS to Luminex microspheres without affecting the antigenicity of a broad set of PnPS. Synonyms: DMTMM; DMT-MM; kunishima coupling reagent; dmt-mm; Morpholinium, 4-(4,6-dimethoxy-1,3,5-triazin-2-yl)-4-methyl-, chloride; J-650384; 4-(4,6-dimethoxy-[1,3,5]triazin-2-yl)-4-methyl-morpholin-4-ium chloride; dmtmm chloride; ACMC-209j5l; SCHEMBL28467; CTK3J8302. Grades: ≥ 95%. CAS No. 3945-69-5. Molecular formula: C10H17ClN4O3. Mole weight: 276.72. | |
| 4,6-Dichloropyrimidin-5-amine | Organic ligands can be prepared through Suzuki cross-coupling reaction between 4,6-Dichloropyrimidin-5-amine and dimethyl(5-pinyl)isophthalate [1]. Uses: Scientific research. Group: Biochemical assay reagents. CAS No. 5413-85-4. Pack Sizes: 5 g; 10 g. Product ID: HY-W001987. | |
| 4-(Diphenylamino)phenylboronic acid pinacol ester | 4-(Diphenylamino)phenylboronic acid pinacol ester is an aryl boronic acid ester that is majorly used in organic synthesis. It can be used in the transition metal-catalyzed Suzuki-Miyaura cross-coupling reaction due to its low toxicity and unique reactivity. It is an electron rich boronic acid ester that can also be used in protodeboronation. Uses: 4-(diphenylamino)phenylboronic acid pinacol ester may be used to synthesize 4-(2,2' -bithiophen-5-yl)- 5-phenylpyrimidine for potential usage in the development of sensing devices for the detection of nitroaromatic explosives. it can also be used in the synthesis of oligothiophene (electron donating group) for the fabrication of dye sensitized solar cells (dsscs). Group: Synthetic tools and reagents. Alternative Names: Diphenyl-[4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-phenyl]-amine, N-(4-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl-N-phenylbenzenamine. Pack Sizes: Packaging 1, 5 g in glass bottle. Product ID: N,N-diphenyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline. Molecular formula: 371.28. Mole weight: C24H26BNO2. CC1 (C)OB (OC1 (C)C)c2ccc (cc2)N (c3ccccc3)c4ccccc4. 1S/C24H26BNO2/c1-23 (2) 24 (3, 4) 28-25 (27-23) 19-15-17-22 (18-16-19) 26 (20-11-7-5-8-12-20) 21-13-9-6-10-14-21/h5-18H, 1-4H3. VKSWIFGDKIEVFZ-UHFFFAOYSA-N. | |
| 4-Formylphenylboronic acid | Reagent used for: Palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water ; Copper-mediated ligandless aerobic fluoroalkylation of arylboronic acids with fluoroalkyl iodides ; Ligand-free copper-catalyzed coupling of nitro arenes with arylboronic acids ; Triethylamine-catalyzed three-component Hantzsch condensations ; Copper-catalyzed nitrations ; Oxidative mono-cleavage of dialkenes catalyzed by Trametes hirsuta ; Palladacycle-catalyzed cross-coupling of arylboronic acids with carboxylic anhydrides or acyl chlorides ; Palladium-catalyzed aerobic oxidative cross-coupling reactions Reagent used in Preparation of; Sensitizers with dithiafulvenyl unit as electron donor for high-efficiency dye-sensitized solar cells; A novel protein synthesis inhibitor active against Gram-positive bacteria. Synonyms: Boronic acid, (4-formylphenyl)-; 4-Boronobenzaldehyde; p-formylphenylboronic acid; MFCD00151823; 4-benzaldehyde boronic acid; 4-(Dihydroxyboryl)benzaldehyde; CHEMBL140254. Grades: 95 %. CAS No. 87199-17-5. Molecular formula: C7H7BO3. Mole weight: 149.94. | |
| 5'-Hexyl-2,2'-bithiophene-5-boronic acid pinacol ester | 5'-Hexyl-2,2'-bithiophene-5-boronic acid pinacol ester. Uses: Reagent use for suzuki-miyaura cross-coupling reactions and shape-shifting in contorted dibenzotetrathienocoronenes oligothiophene self-assembly induction into fibers with tunable shape and function stille coupling and p-conjugated packing structure and hole mobility of bithiophene-bithiazole copolymers with alkyl-thiophene side chains reagent used in preparation of solution-processed ambipolar fi. Group: Saltsynthetic tools and reagents. Alternative Names: 2-(5'-Hexyl-2,2'-bithien-5-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane,4,4,5,5-Tetramethyl-2-[5'-hexyl-2,2'-bithien-5-yl]-1,3,2-dioxaborolane. CAS No. 579503-59-6. Pack Sizes: 1, 5 g in glass bottle. Product ID: 2-[5-(5-hexylthiophen-2-yl)thiophen-2-yl]-4,4,5,5-tetramethyl-1,3,2-dioxaborolane. Molecular formula: 376.38. Mole weight: C20H29BO2S2. CCCCCCc1ccc (s1)-c2ccc (s2)B3OC (C) (C)C (C) (C)O3. 1S / C20H29BO2S2 / c1-6-7-8-9-10-15-11-12-16 (24-15) 17-13-14-18 (25-17) 21-22-19 (2, 3) 20 (4, 5) 23-21 / h11-14H, 6-10H2, 1-5H3, XTTRNSNHDCYSEL-UHFFFAOYSA-N. XTTRNSNHDCYSEL-UHFFFAOYSA-N. | |
| 6-Cl-HOBt | Reagent in peptide synthesis, has also been introduced into solid-phase synthesis. Uses: Peptide Synthesis. Group: Coupling Reagents. Alternative Names: 6-Chloro-1-hydroxybenzotriazole. CAS No. 26198-19-6. |  Luxembourg Bio Technologies |
| 6-Cl-HOBt in AcN | Designed to limit epimerization and increase efficiency during peptide synthesis and to ensure easy of use and safe shipping. Uses: Peptide Synthesis. Group: Coupling Reagents. Alternative Names: 6-Cl-Hydroxybenzotriazole in Acetonitrile. CAS No. 26198-19-6. | Luxembourg Bio Technologies |
| 6-Cl-HOBt in DMF | Designed to limit epimerization and increase efficiency during peptide synthesis and to ensure easy of use and safe shipping. Uses: Peptide Synthesis. Group: Coupling Reagents. Alternative Names: 6-Cl-Hydroxybenzotriazole in N,N -Dimethylformamide. CAS No. 26198-19-6. | Luxembourg Bio Technologies |
Our database is helping our users find suppliers everyday.
