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 | |
|---|---|---|
| 10-(2-Tetrahydropyranyloxy)-8-decynoic acid | Alkynes. CAS No. 1053656-74-8. Molecular formula: C16H10. Mole weight: 268.35. Catalog: ACM1053656748. |  |
| 10-Undecynoyl-OSu | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. Alternative Names: 10-Undecynoic acid succinimidyl ester. CAS No. 1006592-57-9. Molecular formula: C15H21NO4. Mole weight: 279.33. IUPACName: (2,5-Dioxopyrrolidin-1-yl) undec-10-ynoate. Canonical SMILES: C#CCCCCCCCCC(=O)ON1C(=O)CCC1=O. Density: 1.13±0.1 g/cm3(Predicted). Catalog: CCR1006592579. | |
| 1,1'-Bis(dimethylsilyl)ferrocene | Catalytic co-initiator in free radical photopolymerization and free radical promoted cationic polymerization reactions Reactant for: Hydrosilylataion and hydroboration reactions Platinum/nickel catalyzed selective hydrosilylation of alkynes and alkenes Iron-catalyzed dehydrogenative coupling reactions Hydrosilylation and double silylation of carbonyl compounds. Group: Polymer/macromolecule. Alternative Names: 1,1-BIS(DIMETHYLSILYL)FERROCENE;1,1-Bis(dimethylsilyl)ferrocene 97%;Ferrocene,1,1-bis(dimethylsilyl)-. CAS No. 1295-15-4. Molecular formula: C14H22FeSi2 10*. Mole weight: 302.34. Catalog: ACM1295154. | |
| 1,1'-Bis(diphenylphosphino)ferrocene | Ligand for Pd-catalyzed cross-coupling. Useful ligand for Pd-catalyzed carbon-nitrogen and carbon-oxygen bond forming procedures. Ligand for Ni-catalyzed amination of aryl chlorides. Ligand for Pd-catalyzed conversion of aryl halides to aryl nitriles. Ligand for Ni-catalyzed Suzuki reactions. Ni-catalyzed hydroamination of 1,3-dienes. Pd-catalyzed hydrocarbonation and hydroamination of 3,3-dihexylcyclopropene. Pd-catalyzed γ-arylation of β,γ-unsaturated ketones. Ligand for Ru-catalyzed reduction of nitriles to primary amines. Ligand for Rh-catalyzed alkyne head-to-tail dimerization. Ligand for Rh-catalyzed cross-coupling Ligand for Rh-catalyzed olefin isomerization Ligand for Ni or Rh-catalyzed borylation Ligand for regioselective Pd-catalyzed hydrophosphinylation of terminal alkynes to form branched alkenes. Group: Organic phosphine compounds. Alternative Names: 1,1'-Ferrocenediyl-bis(diphenylphosphine); DPPF. CAS No. 12150-46-8. Molecular formula: C34H28FeP2. Mole weight: 554.38. Appearance: Solid. Purity: 0.98. IUPACName: 1,1-Bis(diphenylphosphino)ferrocene. Catalog: ACM12150468-1. | |
| 1,2,4,6-Tetra-O-acetyl-3-azido-3-deoxy-D-glucopyranose | 1,2,4,6-Tetra-O-acetyl-3-azido-3-deoxy-D-glucopyranose, a highly versatile azido sugar, finds wide application in the synthesis of glycoconjugates, including glycolipids, glycopeptides, and oligosaccharides. Its capacity to engage with alkynes through click chemistry makes it a potent investigative tool for studying glycosylation and also holds considerable promise in the treatment of diverse inflammatory and autoimmune disorders. Consequently, this compound promises to be indispensable to a range of cutting-edge scientific endeavors. |  |
| [1, 3-Bis (2, 6-di-i-propylphenyl)imidazol-2-ylidene][bis (trifluoromethanesulfonyl)imide]gold (I), min. 95% | Gold catalyst used for the hydroarylating cyclization of 1,2-bis(2-iodoethynyl)benzenes. Gold catalyst used for the carbocyclization of phenols with a terminal alkyne. Intermolecular C-H activation through the gold(I)-catalyzed reaction of iodoalkynes. Reaction of ynamide with benzyl azides. Group: Gold catalysts. CAS No. 951776-24-2. Molecular formula: C29H36AuF6N3O4S2. Mole weight: 865.7. Catalog: ACM951776242. | |
| 1,3-Bis(2,6-di-i-propylphenyl)imidazol-2-ylidenegold(I) hydroxide, min. 97% | Catalyst used for the carboxylation of C-H bonds. Catalyst used for the hydrofluorination of alkynes. Gold-catalyzed synthesis of sulfinate derivatives Effective catalyst for the carboxylation/cyclization of propargylamines with carbon dioxide. Catalyst used for the polymerization of racemic β-butyrolactones. Catalyst used for the intermolecular mono and dihydroamination of activated alkenes. Group: Gold catalysts. Alternative Names: MFCD22666054;1,3-Bis(2,6-di-i-propylphenyl)imidazol-2-ylidenegold(I) hydroxide;1240328-73-7. CAS No. 1240328-73-7. Molecular formula: C27H38AuN2O. Mole weight: 603.581g/mol. IUPACName: 1,3-bis[2,6-di(propan-2-yl)phenyl]imidazole;gold;hydrate. Canonical SMILES: CC (C)C1=C (C (=CC=C1)C (C)C)N2C=CN ([C]2)C3=C (C=CC=C3C (C)C)C (C)C. O. [Au]. Catalog: ACM1240328737. | |
| 1,3-Bis(2,6-di-isopropylphenyl)imidazol-2-ylidenegold(I) chloride, 95% | Catalyst used for rearrangement of allylic acetates. Catalyst used for alkane carbon-hydrogen bond functionalization. Catalyst used for room temperature hydroamination of N-alkenyl ureas. Catalyst used for hydration of alkynes. Group: Gold series of catalysts. Alternative Names: 852445-83-1; SC10711; 1,3-Bis(2,6-diisopropylphenyl)imidazol-2-ylidene gold(I)chloride; {1,3-Bis[2,6-di(propan-2-yl)phenyl]-1,3-dihydro-2H-imidazol-2-ylidene}(chloro)gold; AKOS015951030; 1,3-Bis(2,6-diisopropylphenyl-imidazol-2-ylidene)gold(I) chloride; (1,3-Bis(2,6-diisopropylphenyl)-1,3-dihydro-2H-imidazol-2-ylidene)(chloro)gold. CAS No. 852445-83-1. Molecular formula: C27H36AuClN2. Mole weight: 621.016g/mol. IUPACName: [1,3-bis[2,6-di(propan-2-yl)phenyl]imidazol-2-ylidene]-chlorogold. Canonical SMILES: CC (C)C1=C (C (=CC=C1)C (C)C)N2C=CN (C2=[Au]Cl)C3=C (C=CC=C3C (C)C)C (C)C. Catalog: ACM852445831. | |
| 1-Azido-3,6,9,12-tetraoxapentadec-14-yne | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. Alternative Names: Azido-PEG4-propargyl. CAS No. 1192590-91-2. Molecular formula: C11H19N3O4. Mole weight: 257.29. IUPACName: 3-[2-[2-[2-(2-Azidoethoxy)ethoxy]ethoxy]ethoxy]prop-1-yne. Canonical SMILES: C#CCOCCOCCOCCOCCN=[N+]=[N-]. Catalog: CCR1192590912. | |
| 1-Butyne-3,3,4,4,4-d5 | 1-Butyne-3,3,4,4,4-d5 is deuterium labelled 1-Butyne. 1-Butyne can be utilized for stereocontrolled synthesis such as controlled hydrogenation of terminal alkynes. It can also be used to synthesize polyene natural products by iterative cross coupling. Group: Biochemicals. Grades: Highly Purified. CAS No. 60173-50-4. Pack Sizes: 100mL, 250mL. Molecular Formula: C4HD5, Molecular Weight: 59.12. US Biological Life Sciences. |  Worldwide |
| 1-Hexyn-3-ol | Alkynes. CAS No. 105-31-7. Molecular formula: C6H10O. Mole weight: 98.14. Purity: N/A. Catalog: ACM105317. | |
| 1-Phenyl-3-pyrrolidinone | 1-Phenyl-3-pyrrolidinone is used as a reagent in the synthesis of a series of non-classical antifolates which were evaluated for their in vitro cytotoxicity. Also used in the preparation of azetidine- and pyrrolidine-containing alkynes as mGluR5 regulators. Group: Biochemicals. Grades: Highly Purified. CAS No. 128120-02-5. Pack Sizes: 250mg, 2.5g. Molecular Formula: C10H11NO, Molecular Weight: 161.199999999999. US Biological Life Sciences. | Worldwide |
| 1-Phenyl-3-pyrrolidinone-d5 | 1-Phenyl-3-pyrrolidinone-d5 is the isotope labelled analog of 1-Phenyl-3-pyrrolidinone (P336730); a reagent used in the synthesis of a series of non-classical antifolates which were evaluated for their in vitro cytotoxicity. Also used in the preparation of azetidine- and pyrrolidine-containing alkynes as mGluR5 regulators. Group: Biochemicals. Grades: Highly Purified. Pack Sizes: 2.5mg, 25mg. Molecular Formula: C10H6D5NO, Molecular Weight: 166.23. US Biological Life Sciences. | Worldwide |
| 1-Tetradecyne | 1-Tetradecyne is used in addition reactions of alkynes like hydrogenation, halogenation, hydrohalogenation, hydration reactions and others. Group: Biochemicals. Grades: Highly Purified. CAS No. 765-10-6. Pack Sizes: 1ml, 2.5ml. Molecular Formula: C14H26, Molecular Weight: 194.36. US Biological Life Sciences. | Worldwide |
| 2-(2-Fluorophenyl)-3-butyn-2-ol | Alkynes. CAS No. 104684-14-2. Molecular formula: C9H14. Mole weight: 164.18. Catalog: ACM104684142. | |
| 2,5-Dioxopyrrolidin-1-yl 11-oxo-4,7,13-trioxa-10-azahexadec-15-yn-1-oate | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. Alternative Names: Propargyl-O-C1-amido-PEG2-C2-NHS ester. CAS No. 2101206-30-6. Molecular formula: C16H22N2O8. Mole weight: 370.35. IUPACName: (2,5-Dioxopyrrolidin-1-yl) 3-[2-[2-[ (2-prop-2-ynoxyacetyl) amino]ethoxy]ethoxy]propanoate. Canonical SMILES: C#CCOCC (=O)NCCOCCOCCC (=O)ON1C (=O)CCC1=O. Catalog: CCR2101206306. | |
| 2,5-Dioxopyrrolidin-1-yl 2-(prop-2-yn-1-yloxy)acetate | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. Alternative Names: 2-(Propynyloxy)acetic acid-NHS-ester. CAS No. 1858242-47-3. Molecular formula: C9H9NO5. Mole weight: 211.17. IUPACName: (2,5-Dioxopyrrolidin-1-yl) 2-prop-2-ynoxyacetate. Canonical SMILES: C#CCOCC(=O)ON1C(=O)CCC1=O. Catalog: CCR1858242473. | |
| 2-Amino-5-fluorobenzaldehyde | 2-Amino-5-fluorobenzaldehyde is a building block used in various synthetic preparations. It was used as a reactant in the stereoselective preparation of aryltetra hydroquinolines via gold-phosphine catalyzed heterocyclization of aminobenzaldehyde with alkynes. Group: Biochemicals. Grades: Highly Purified. CAS No. 146829-56-3. Pack Sizes: 50mg, 100mg. Molecular Formula: C7H6FNO, Molecular Weight: 139.13. US Biological Life Sciences. | Worldwide |
| 2-Amino-5-methylnicotinaldehyde | 2-Amino-5-methylnicotinaldehyde is a reactant used in the preparation of naphthyridines by Cu-catalyzed hydroamination / Friedlander reaction with terminal alkynes. Group: Biochemicals. Grades: Highly Purified. CAS No. 1023814-35-8. Pack Sizes: 10mg, 25mg. Molecular Formula: C7H8N2O, Molecular Weight: 136.15. US Biological Life Sciences. | Worldwide |
| 2-Amino-5-methylnicotinaldehyde | A reagent used in the preparation of naphthyridines by Cu-catalyzed hydroamination/Friedlander reaction with terminal alkynes. Synonyms: 2-amino-5-methylpyridine-3-carbaldehyde. CAS No. 1023814-35-8. Molecular formula: C7H8N2O. Mole weight: 136.15. | |
| 2-Dicyclohexyl(2', 6'-dimethoxybiphenyl)phosphine gold(I) bis(trifluoromethylsulfonyl)imide | Catalyst used in the selective hydration of substituted alkynes at room temperatures. Catalyst used in the hydroarylating/aromatization of arene-diynes. Highly-efficient and regio-selective catalyst for the selective carbonyl migration in alkynyl-substituted indole-3-carboxamides. Intermolecular gold(I) catalyzed alkyne carboalkoxylation reactions for the multicomponent assembly of β-alkoxy ketones. Gold(I)-catalyzed hydration of alkynylphosphonates: Efficient access to β-ketophosphonates. Gold-catalyzed intramolecular hydroamination reaction. Group: Gold catalysts. Alternative Names: MFCD21608485; 1121960-90-4; Bis(trifluoromethanesulfonyl)imide(2-dicyclohexylphosphino-2', 6'-dimethoxy-1, 1'-biphenyl)gold(I). CAS No. 1121960-90-4. Molecular formula: C28H36AuF6NO6PS2+. Mole weight: 888.648g/mol. IUPACName: bis(trifluoromethylsulfonyl)azanide; dicyclohexyl-[2-(2, 6-dimethoxyphenyl)phenyl]phosphanium; gold(1+). Canonical SMILES: COC1=C (C (=CC=C1)OC)C2=CC=CC=C2[PH+] (C3CCCCC3)C4CCCCC4. C (F) (F) (F)S (=O) (=O)[N-]S (=O) (=O)C (F) (F)F. [Au+]. Catalog: ACM1121960904. | |
| 2'-Dicyclohexylphosphino-2,6-di-i-propyl-4-sulfonato-1,1'-biphenyl hydrate sodium salt | Water soluble catalyst for Sonogashira coupling reactions Water soluble catalyst for coupling of benzyl chloride and terminal alkynes. Water soluble ligand for cyanation of aryl chlorides and aryl sulfonates with potassium ferrocyanide. Group: Organic phosphine compounds. Alternative Names: AK122632; C30H44NaO4PS; Sodium 2'-(dicyclohexylphosphino)-2,6-diisopropyl-[1,1'-biphenyl]-4-sulfonate hydrate; sodium; DTXSID00855870; Sodium 2'-(dicyclohexylphosphanyl)-2,6-di(propan-2-yl)[1,1'-biphenyl]-4-sulfonate--water (1/1/1); sodium 2'-(dicyclohexylphosphanyl)-2,6-diisopropyl-[1,1'-biphenyl]-4-sulfonate hydrate; 2'-DICYCLOHEXYLPHOSPHINO-2,6-DI-I-PROPYL-4-SULFONATO-1,1'-BIPHENYL HYDRATE SODIUM SALT; SCHEMBL2673886; XPHOS-SO3NA HYDRATE. CAS No. 870245-84-4. Molecular formula: C30H44NaO4PS. Mole weight: 554.702g/mol. IUPACName: sodium;4-(2-dicyclohexylphosphanylphenyl)-3,5-di(propan-2-yl)benzenesulfonate;hydrate. Canonical SMILES: CC (C)C1=CC (=CC (=C1C2=CC=CC=C2P (C3CCCCC3)C4CCCCC4)C (C)C)S (=O) (=O)[O-]. O. [Na+]. Catalog: ACM870245844. | |
| 2-Heptyn-1-ol | Alkynes. CAS No. 1002-36-4. Molecular formula: C7H12O. Mole weight: 112.17. Purity: 0.98. Catalog: ACM1002364. | |
| 2-Heptyne | Alkynes. CAS No. 1119-65-9. Molecular formula: C7H12. Mole weight: 96.17. Purity: >99.0%(GC). Catalog: ACM1119659. | |
| 2-Phenyl-3-butyn-2-ol | Alkynes. CAS No. 127-66-2. Molecular formula: C6H5C(CH3)(OH)C?CH. Mole weight: 146.19. Purity: ≥98%. Catalog: ACM127662. | |
| (2-Pyridyldithio)-PEG4-propargyl | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. CAS No. 2170240-99-8. Molecular formula: C16H23NO4S2. Mole weight: 357.49. IUPACName: 2- [2- [2- [2- (2-Prop-2-ynoxyethoxy) ethoxy] ethoxy] ethyldisulfanyl] pyridine. Canonical SMILES: C#CCOCCOCCOCCOCCSSC1=CC=CC=N1. Catalog: CCR2170240998. | |
| (2S,4S)-Fmoc-L-pro(4-NHPoc)-OH | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. Alternative Names: (2S,4S)-Fmoc-pro(4-NH-poc). CAS No. 2451202-17-6. Molecular formula: C24H22N2O6. Mole weight: 434.44. IUPACName: (2S,4S)-1-(9H-Fluoren-9-ylmethoxycarbonyl)-4-(prop-2-ynoxycarbonylamino)pyrrolidine-2-carboxylic acid. Canonical SMILES: C#CCOC (=O)NC1CC (N (C1)C (=O)OCC2C3=CC=CC=C3C4=CC=CC=C24)C (=O)O. Catalog: CCR2451202176. | |
| 2-tert-Butyldimethylsiloxybut-3-yne | Alkynes. CAS No. 125494-93-1. Mole weight: 184.35. Catalog: ACM125494931. | |
| 3-(2-(2-Bromoethoxy)ethoxy)prop-1-yne | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. Alternative Names: Propargyl-PEG2-bromide. CAS No. 1287660-82-5. Molecular formula: C7H11BrO2. Mole weight: 207.07. IUPACName: 3-[2-(2-Bromoethoxy)ethoxy]prop-1-yne. Canonical SMILES: C#CCOCCOCCBr. Catalog: CCR1287660825. | |
| 3-[2-(2-Iodoethoxy)-ethoxy]-propyne | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. Alternative Names: Alkyne-PEG2-iodide. CAS No. 1234387-33-7. Molecular formula: C7H11IO2. Mole weight: 254.07. IUPACName: 3-[2-(2-Lodoethoxy)ethoxy]prop-1-yne. Canonical SMILES: C#CCOCCOCCI. Density: 1.593±0.06 g/cm3(Predicted). Catalog: CCR1234387337. | |
| 3,3-Diethoxy-1-propyne | Alkynes. CAS No. 10160-87-9. Molecular formula: C7H12O. Mole weight: 128.17. Catalog: ACM10160879. | |
| 3,6,9,12,15,18,21,24,27,30-Decaoxatritriacont-32-yn-1-ol | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. CAS No. 2378150-09-3. Molecular formula: C23H44O11. Mole weight: 496.59. IUPACName: 2- [2- [2- [2- [2- [2- [2- [2- [2- (2-Prop-2-ynoxyethoxy) ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethanol. Canonical SMILES: C#CCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCO. Catalog: CCR2378150093. | |
| 3-Ethynyl perylene | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. Alternative Names: 3-Perylenylacetylene. CAS No. 132196-66-8. Molecular formula: C22H12. Mole weight: 276.33. IUPACName: 3-Ethynylperylene. Canonical SMILES: C#CC1=C2C=CC=C3C2=C (C=C1)C4=CC=CC5=C4C3=CC=C5. Catalog: CCR132196668. | |
| 3-Hexyn-1-ol | Alkynes. CAS No. 1002-28-4. Molecular formula: C6H10O. Mole weight: 98.14. Purity: >97.0%(GC). Catalog: ACM1002284. | |
| 3-Hexyn-2-ol | Alkynes. CAS No. 109-50-2. Molecular formula: C6H9I. Mole weight: 98.14. Catalog: ACM109502. | |
| 3-Hydroxyphenylacetylene | Alkynes. CAS No. 10401-11-3. Mole weight: 118.13. Catalog: ACM10401113. | |
| 3-Methyl-1-pentyn-3-amine hydrochloride | Alkynes. Alternative Names: 3-AMINO-3-METHYL-1-PENTYNE HCL;1-Ethyl-1-methyl-prop-2-ynylamine hydrochloride. CAS No. 108575-32-2. Molecular formula: C6H10O. Mole weight: 133.62. Purity: 0.96. IUPACName: 3-methylpent-1-yn-3-amine;hydrochloride. Catalog: ACM108575322. | |
| 3-Pentyn-1-ol | Alkynes. CAS No. 10229-10-4. Molecular formula: C5H8O. Mole weight: 84.12. Purity: >98.0%(GC). Catalog: ACM10229104. | |
| 4-Hydroxynonenal alkyne | 4-Hydroxynonenal alkyne (4-HNE alkyne) is a click chemical reagent containing alkynes. 4-Hydroxynonenal alkyne induces heme oxygenase and cell apoptosis in colon cancer (RKO) cells [1]. Uses: Scientific research. Group: Signaling pathways. Alternative Names: 4-HNE alkyne. CAS No. 1011268-23-7. Pack Sizes: 100 μg (6.57 mM * 100 μL in Methyl acetate). Product ID: HY-113803. |  |
| 4-Pentynoyl-val-ala-PAB | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. Alternative Names: 4-Pentynoyl-val-ala-PAB-OH. CAS No. 1956294-75-9. Molecular formula: C20H27N3O4. Mole weight: 373.4. IUPACName: (2S)-N-[(2S)-1-[4-(Hydroxymethyl)anilino]-1-oxopropan-2-yl]-3-methyl-2-(pent-4-ynoylamino)butanamide. Canonical SMILES: CC (C)C (C (=O)NC (C)C (=O)NC1=CC=C (C=C1)CO)NC (=O)CCC#C. Catalog: CCR1956294759. | |
| 4-Pentynoyl-val-ala-PAB-PNP | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. CAS No. 1956294-76-0. Molecular formula: C27H30N4O8. Mole weight: 538.5. IUPACName: [4- [ [ (2S) -2- [ [ (2S) -3-Methyl-2- (Pent-4-ynoylamino) butanoyl] amino] propanoyl] amino] phenyl] methyl (4-nitrophenyl) carbonate. Canonical SMILES: CC (C)C (C (=O)NC (C)C (=O)NC1=CC=C (C=C1)COC (=O)OC2=CC=C (C=C2)[N+] (=O)[O-])NC (=O)CCC#C. Catalog: CCR1956294760. | |
| 5-Hexynoic NHS ester | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. Alternative Names: 2,5-Dioxopyrrolidin-1-yl hex-5-ynoate. CAS No. 906564-59-8. Molecular formula: C10H11NO4. Mole weight: 209.2. IUPACName: (2,5-Dioxopyrrolidin-1-yl) hex-5-ynoate. Canonical SMILES: C#CCCCC(=O)ON1C(=O)CCC1=O. Catalog: CCR906564598. | |
| 6-O-2-Propyn-1-yl-D-galactose | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. Alternative Names: D-Galactose, 6-O-2-propyn-1-yl-. CAS No. 881895-59-6. Molecular formula: C9H14O6. Mole weight: 218.2. IUPACName: (2R,3S,4S,5R)-2,3,4,5-Tetrahydroxy-6-prop-2-ynoxyhexanal. Canonical SMILES: C#CCOCC(C(C(C(C=O)O)O)O)O. Density: 1.398±0.06 g/cm3(Predicted). Catalog: CCR881895596. | |
| 6-O-Propynyl-2'-deoxyguanosine | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. Alternative Names: Guanosine, 2'-deoxy-6-O-2-propyn-1-yl-. CAS No. 1640051-47-3. Molecular formula: C13H15N5O4. Mole weight: 305.29. Purity: 99%+. IUPACName: (2R,5R)-5-(2-Amino-6-prop-2-ynoxypurin-9-yl)-2-(hydroxymethyl)oxolan-3-ol. Canonical SMILES: C#CCOC1=NC (=NC2=C1N=CN2C3CC (C (O3)CO)O)N. Catalog: CCR1640051473. | |
| 7-Octynoic acid | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. Alternative Names: Oct-7-ynoicacid. CAS No. 10297-09-3. Molecular formula: C8H12O2. Mole weight: 140.18. Appearance: Liquid. Purity: 98%+. IUPACName: Oct-7-ynoic acid. Canonical SMILES: C#CCCCCCC(=O)O. Density: 1.045 g/cm3(Predicted). Catalog: CCR10297093. | |
| 9,9-Dimethyl-4,5-bis(di -tert-butylphosphino) -9H-xanthene | Ligand used in the cobalt-catalyzed alkenylzincation of unfunctionalized alkynes. Ligand used in the cobalt-catalyzed alkylboration of alkenes. Ligand used in the palladium-catalyzed N-alkylation of amines using primary and secondary alcohols. Ligand used in the palladium-catalyzed methylation of alkynyl C(sp)-H bonds with dimethyl sulfonium ylides. Group: Organic phosphine compounds. Alternative Names: AX8240548; ditert-butyl-(5-ditert-butylphosphanyl-9,9-dimethylxanthen-4-yl)phosphane; SCHEMBL1315091; 4,5-bis(di-t-butylphosphino)-9,9-dimethylxanthene; 9,9-Dimethyl-4,5-bis(di-tert-butylphosphino)xanthene; FT-0728449; ZINC12359415; t-Bu-Xantphos; CS-W009619; DB-009564. CAS No. 856405-77-1. Molecular formula: C31H48OP2. Mole weight: 498.672g/mol. IUPACName: ditert-butyl-(5-ditert-butylphosphanyl-9,9-dimethylxanthen-4-yl)phosphane. Canonical SMILES: CC1 (C2=C (C (=CC=C2)P (C (C) (C)C)C (C) (C)C)OC3=C1C=CC=C3P (C (C) (C)C)C (C) (C)C)C. Catalog: ACM856405771. | |
| (9,9-Dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) | Ligand used for the hydroformylation of alkenes. Ligand used in the intermolecular coupling of amides and hydrazones with aryl halides. Ligand used in the intermolecular coupling of amides with aryl halides or triflates. Ligand used in the coupling of heteroarylamines and aryl halides. Ligand used in the hydrophosphinylation of alkenes and alkynes. Ligand used for the Au(I)-catalyzed dehydrogenative silation of alcohols. Ligand used for the sulfinylation of aryl iodides. Ligand used for the Pd-catalyzed carbonylation reaction of aryl bromides and amines. Ligand used for the Ni-cataltzed alkynylcyanation of alkynes. Ligand used for the Pd-catalyzed N-arylation of 3-amino-1H-pyrazole. Ligand used for the Rh-catalyzed dehydrogenation borylation of cyclic alkenes. Ligand used for the Pd-catalyzed intermolecular coupling of H-Phosphonate diesters with benzyl halides. Ligand used for the Pd-catalyzed one pot synthesis of 4-aryl-1H-1,2,3-triazoles. Ligand used for the Pd-catalyzed intermolecular addition of formamides to alkynes. Ligand used for the Pd-catalyzed decarboxylative couplings of 2-(2-azaaryl)acetates with aryl halides and triflates. Ligand used for the Pd-catalyzed benzylic arylation of 2-methyl azaarenes Ligand used for the Pd-catalyzed α-arylation of heteroaromatic ketones. Ligand used for the Pd-catalyzed direct alkynlation of both azoles and azolines. Ligand used fo | |
| Ac4GalNAl | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. Alternative Names: 2-Deoxy-2-[(1-oxo-4-pentyn-1-yl)amino]-1,3,4,6-tetraacetate-D-galactopyranose. CAS No. 1673590-09-4. Molecular formula: C19H25NO10. Mole weight: 427.4. IUPACName: [(2R,3R,4R,5R,6S)-3,4,6-Triacetyloxy-5-(pent-4-ynoylamino)oxan-2-yl]methyl acetate. Canonical SMILES: CC (=O)OCC1C (C (C (C (O1)OC (=O)C)NC (=O)CCC#C)OC (=O)C)OC (=O)C. Density: 1.28±0.1 g/cm3(Predicted). Catalog: CCR1673590094. | |
| Ac4GlcNAlk | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. CAS No. 1361993-37-4. Molecular formula: C19H25NO10. Mole weight: 427.4. IUPACName: [(2R,3S,4R,5R)-3,4,6-Triacetyloxy-5-(pent-4-ynoylamino)oxan-2-yl]methyl acetate. Canonical SMILES: CC (=O)OCC1C (C (C (C (O1)OC (=O)C)NC (=O)CCC#C)OC (=O)C)OC (=O)C. Density: 1.28±0.1 g/cm3(Predicted). Catalog: CCR1361993374. | |
| Acetonitrilebis [2-diphenylphosphino-6-t-butylpyridine] cyclopentadienylruthenium (II) hexafluorophosphate, min. 98% | Catalyst used for the Anti-Markovnikov hydration of terminal alkynes to aldehydes. Catalyst used for cyclization and hydration of phenyl alkynes to functionalized indoles and benzofurans. Group: Ruthenium series catalysts. Alternative Names: ACETONITRILEBIS [2-DIPHENYLPHOSPHINO-6-T-BUTYLPYRIDINE] CYCLOPENTADIENYLRUTHENIUM (II) HEXAFLUOROPHOSPHATE; Acetonitrilebis [2-diphenylphosphino-6-t-butylpyridine] cyclopentadienylruthenium (II) hexafluorophosphate, min. 98% ; Acetonitrilebis [2-diphenylphosphino-6-. CAS No. 776230-17-2. Molecular formula: C49H52F6N3P3Ru. Mole weight: 990.94. Appearance: yellow powder. Purity: 0.98. IUPACName: acetonitrile; (6-tert-butylpyridin-2-yl)-diphenylphosphane; cyclopentane; ruthenium(1+); hexafluorophosphate. Canonical SMILES: CC#N. CC (C) (C)C1=NC (=CC=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. CC (C) (C)C1=NC (=CC=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. [CH]1[CH][CH][CH][CH]1. F[P-] (F) (F) (F) (F)F. [Ru+]. Catalog: ACM776230172. | |
| AF488 azide | AF488 is a fluorescent dye. AF488 is a fluorophore pH-insensitive over a broad pH range (from 4 to 10). It has an absorption maximum at 495 nm and an emission maximum at 519 nm in the green spectrum region. The dye is hydrophilic and can be used to introduce the fluorescent label into various molecules, including proteins and antibodies. Conjugates of molecules with AF488 have high brightness and photostability and are commonly used in flow cytometry and microscopy. This allows the detection of biological objects with high sensitivity at a longer imaging time.,AF488 azide interacts with alkynyl derivatives of biomolecules in Click Chemistry reactions either in the presence of copper (I) catalyst (with terminal alkynes) or without catalyst (with cyclooctynes), leading to the formation of stable adducts. Grades: NMR 1H, HPLC-MS (95%). CAS No. 1679326-36-3 (with azidohexyl group). Molecular formula: C36H56N8O10S2. Mole weight: 825.01. | |
| Ald-benzyl-amide-PEG4-propargyl | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. Alternative Names: Ald-Ph-amido-PEG4-propargyl. CAS No. 1969299-27-1. Molecular formula: C19H25NO6. Mole weight: 363.4. IUPACName: 4-Formyl-N-[2-[2-[2- (2-prop-2-ynoxyethoxy) ethoxy]ethoxy]ethyl]benzamide. Canonical SMILES: C#CCOCCOCCOCCOCCNC (=O)C1=CC=C (C=C1)C=O. Catalog: CCR1969299271. | |
| Aldehyde-benzyl-PEG5-alkyne | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. Alternative Names: 4-(3,6,9,12-Tetraoxahexadec-15-yn-1-yloxy)benzaldehyde. CAS No. 1378928-83-6. Molecular formula: C18H24O6. Mole weight: 336.38. IUPACName: 4-[2-[2-[2- (2-But-3-ynoxyethoxy) ethoxy]ethoxy]ethoxy]benzaldehyde. Canonical SMILES: C#CCCOCCOCCOCCOCCOC1=CC=C(C=C1)C=O. Density: 1.123±0.06 g/cm3(Predicted). Catalog: CCR1378928836. | |
| alkyne-cholesterol | alkyne-cholesterol is a modified lipid of omega terminal alkynes. Synonyms: 27-norcholest-5-en-25-yn-3beta-ol. Grades: >99%. CAS No. 1631985-09-5. Molecular formula: C26H40O. Mole weight: 368.60. | |
| Alkyne tyramide | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. Alternative Names: N-(4-Hydroxyphenethyl)pent-4-ynamide. CAS No. 1694495-59-4. Molecular formula: C13H15NO2. Mole weight: 217.26. Appearance: Solid. Purity: 99%+. IUPACName: N-[2-(4-Hydroxyphenyl)ethyl]pent-4-ynamide. Canonical SMILES: C#CCCC(=O)NCCC1=CC=C(C=C1)O. Catalog: CCR1694495594. | |
| Allylpalladium(II) chloride dimer | Precatalyst for the enantioselective hydrosilylation of olefins. Precatalyst for asymmetric allylic alkylation and amination. Used as a palladium source for cross-coupling reactions. Can be used with Trost ligands. Catalyst for the carbostannylation of alkynes. Used as a precatalyst for "-arylation of aldehydes. Group: Palladium series catalysts. Alternative Names: Di-mu-chlorodi-pi-allyldipalladium; NSC 151255; Bis(pi-allylpalladium chloride) (VAN); MFCD00044874 (95%); Bis(mu-chloro)bis(eta3-2-propenyl)dipalladium; AK327212; 12012-95-2; Palladium, di-pi-allyldi-mu-chlorodi- (8CI); Bis((eta3-allyl)(chloro)palladium); SC10406. CAS No. 12012-95-2. Molecular formula: C6H10Cl2Pd2. Mole weight: 365.886g/mol. IUPACName: chloropalladium(1+);prop-1-ene. Canonical SMILES: [CH2-]C=C.[CH2-]C=C.Cl[Pd+].Cl[Pd+]. ECNumber: 234-579-8. Catalog: ACM12012952. | |
| Aminooxy-amido-PEG4-propargyl | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. Alternative Names: Aminooxyacetamide-PEG4-propargyl. CAS No. 2253965-03-4. Molecular formula: C13H24N2O6. Mole weight: 304.34. IUPACName: 2-Aminooxy-N-[2-[2-[2- (2-prop-2-ynoxyethoxy) ethoxy]ethoxy]ethyl]acetamide. Canonical SMILES: C#CCOCCOCCOCCOCCNC(=O)CON. Catalog: CCR2253965034. | |
| APN-C3-PEG4-alkyne | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. Alternative Names: N-(4-((4-(Cyanoethynyl)phenyl)amino)-4-oxobutyl)-4,7,10,13-tetraoxahexadec-15-ynamide. CAS No. 2183440-36-8. Molecular formula: C25H31N3O6. Mole weight: 469.53. IUPACName: N- [4- (2-Cyanoethynyl) phenyl] -4- [3- [2- [2- (2-prop-2-ynoxyethoxy) ethoxy] ethoxy] propanoylamino] butanamide. Canonical SMILES: C#CCOCCOCCOCCOCCC (=O)NCCCC (=O)NC1=CC=C (C=C1)C#CC#N. Catalog: CCR2183440368. | |
| arachidonic acid-alkyne | arachidonic acid-alkyne is a modified lipid containing omega terminal alkynes. Synonyms: 5Z,8Z,11Z,14Z-eicosatetraen-19-ynoic acid. Grades: >99%. CAS No. 1219038-32-0. Molecular formula: C20H28O2. Mole weight: 300.44. | |
| Azido-PEG12-propargyl | CuAAC & SPAAC Click Reactions. Group: Azidesterminal alkynes. CAS No. 2264091-72-5. Molecular formula: C27H51N3O12. Mole weight: 609.71. Catalog: CCR2264091725. | |
| Azido-PEG8-propargyl | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. Alternative Names: 1-Azido-3,6,9,12,15,18,21,24-octaoxaheptacos-26-yne. CAS No. 1196733-06-8. Molecular formula: C19H35N3O8. Mole weight: 433.5. IUPACName: 3- [2- [2- [2- [2- [2- [2- [2- (2-Azidoethoxy) ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] prop-1-yne. Canonical SMILES: C#CCOCCOCCOCCOCCOCCOCCOCCOCCN= [N+]= [N-]. Catalog: CCR1196733068. | |
| Biotin-Azide(≥97% ) | Biotin azide reacts with the terminal alkynes via a copper-catalyzed click reaction, including biomolecules containing alkyne groups through azide-alkyne cycloaddition. Biotin and biotin derivatives can be readily conjugated to various biomolecules through the well-known click chemistry and subsequently detected with streptavidin, avidin or NeutrAvidin biotin-binding protein. Biotin azide can be used to prepare various biotinylated conjugates via Click Chemistry. Click chemistry contains a class of chemical reactions that use bio-orthogonal or biologically unique moieties to label and detect the molecule in mild and aqueous conditions. This reagent allows labeling of various alkynylated molecules, such as DNA, oligonucleotides, and proteins with biotin. Biotin binding to avidin or streptavidin could be used in downstream affinity applications for the isolation of biotinylated molecules or their binding with streptavidin conjugates [1]. Uses: Useful for biotinylation of reagents. Group: Biotinylation reagents. Alternative Names: Biotin-Azide. CAS No. 1006592-62-6. Molecular formula: C27H49N7O7S. Mole weight: 615.79 g/mol. Appearance: To be determined. Purity: ≥97%. IUPACName: N-(6-azidohexyl)-1-(5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamido)-3,6,9,12-tetraoxapentadecan-15-amide. Canonical SMILES: [H][C@@]1 (N2)[C@] ([C@H] (CCCCC (NCCOCCOCCOCCOCCC (NCCCCCCN=[N+]=[N-])=O)=O)SC1) ([H])NC2= | |
| Biotin-PEG11-Azide(≥97% ) | Biotinylation reagent with Azide, and a long 11 PEG spacer. Labels terminal alkynes via a copper-catalyzed "click reaction". Useful for labeling fluorescent dyes with triple bond alkyne groups. Uses: Useful for biotinylation of fluorescent dyes or other compounds with triple bond alkynes via click chemistry. Group: Biotin-peg. Alternative Names: Biotin-PEG11-azide. CAS No. 956494-20-5. Molecular formula: C34H64N6O13S. Mole weight: 796.98 g/mol. Appearance: Solid powder. Purity: ≥97%. IUPACName: N-(35-azido-3,6,9,12,15,18,21,24,27,30,33-undecaoxapentatriacontyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide. Canonical SMILES: O= C1N [C@@] 2 ( [H] ) CS [C@@H] (C CCCC (NCCOCCOCCOCCOCCOCCOCCOCCOCCOCC OCCOCCN= [N + ] = [N-] ) = O) [C@@] 2 ( [H] ) N1. Catalog: BR00028397. | |
| Biotin-PEG3-Azide(≥97% ) | Biotinylation reagent with Azide, and a 3 PEG spacer. Labels terminal alkynes via a copper-catalyzed "click reaction". Useful for labeling fluorescent dyes with triple bond alkyne groups. Uses: Useful for biotinylation of fluorescent dyes or other compounds with triple bond alkynes via click chemistry. Group: Biotin-peg. Alternative Names: Biotin-PEG3-azide. CAS No. 1859110-99-8. Molecular formula: C18H32N6O5S. Mole weight: 444.6 g/mol. Appearance: Solid powder. Purity: ≥97%. IUPACName: N-(2-(2-(2-(2-azidoethoxy)ethoxy)ethoxy)ethyl)-5-((3aS,4S,6aR)-2-oxohexahydro-1H-thieno[3,4-d]imidazol-4-yl)pentanamide. Canonical SMILES: O=C1N[C@@]2 ([H])CS[C@@H] (CCCCC (NCCOCCOCCOCCN=[N+]=[N-])=O)[C@@]2 ([H])N1. Catalog: BR00028319. | |
| Biotin-PEG4-SS-alkyne | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. CAS No. 1260247-54-8. Molecular formula: C29H49N5O8S3. Mole weight: 691.92. IUPACName: 4- [ (3aR, 6aS) -2-Oxo-1, 3, 3a, 4, 6, 6a-hexahydrothieno [3, 4-d] imidazol-4-yl] -N- [2- [2- [2- [2- [3- [2- [ [3- (but-3-ynylamino) -3-oxopropyl] disulfanyl] ethylamino] -3-oxopropoxy] ethoxy] ethoxy] ethoxy] ethyl] butanamide. Canonical SMILES: C#CCCNC (=O)CCSSCCNC (=O)CCOCCOCCOCCOCCNC (=O)CCCC1C2C (CS1)NC (=O)N2. Catalog: CCR1260247548. | |
| Bis-propargyl-PEG11 | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. Alternative Names: Bis-propargyl-PEG11/4, 7, 10, 13, 16, 19, 22, 25, 28, 31, 34, 37-dodecaoxatetraconta-1, 39-diyne. CAS No. 1351373-49-3. Molecular formula: C28H50O12. Mole weight: 578.69. IUPACName: 3- [2- [2- [2- [2- [2- [2- [2- [2- [2- [2- (2-Prop-2-ynoxyethoxy) ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] prop-1-yne. Canonical SMILES: C#CCOCCOCCOCCOCCOCCOCCOCCOCCOCCOCCOC COCC#C. Catalog: CCR1351373493. | |
| Bis-propargyl-PEG8 | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. Alternative Names: 4,7,10,13,16,19,22,25-Octaoxaoctacosa-1,27-diyne. CAS No. 1351373-46-0. Molecular formula: C20H34O8. Mole weight: 402.48. Purity: 98%+. IUPACName: 3- [2- [2- [2- [2- [2- [2- (2-Prop-2-ynoxyethoxy) ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] ethoxy] prop-1-yne. Canonical SMILES: C#CCOCCOCCOCCOCCOCCOCCOCCOCC#C. Catalog: CCR1351373460. | |
| Bis(triphenylphosphine)palladium(II) Dichloride | Bis(triphenylphosphine)palladium(II) Dichloride. Uses: Precatalyst for the carbonylative cyclization of malonate derivatives. catalyst used in the double allylation of activated olefins. precatalyst for the three-component preparation of 3-arylidene- (or 3-alkenylidene) tetrahydrofurans. precatalyst for the homocoupling of terminal alkynes. precatalyst in the cross-coupling of alkynylsilanols and aryl halides. catalyst for direct pd-catalyzed alkynylation of n-fused heterocycles. catalyst for a tandem heck reaction/c-h functionalization. catalyst for direct arylation of tautomerizable heterocycles. Group: Salt. Alternative Names: TRANS-BIS-(TRIPHENYLPHOSPHINE)PALLADIUM DICHLORIDE; 13965-03-2; 28966-81-6; AC1L36TY; SC-01002; LS-192238; bis(triphenylphosphine) palladiuml(II) dichloride; bis(triphenylphosphine) palladium (II) chloride; FC0823; EINECS 237-744-2. CAS No. 13965-03-2. Product ID: palladium(2+); triphenylphosphane; dichloride. Molecular formula: 701.904g/mol. Mole weight: C36H30Cl2P2Pd. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. [Cl-]. [Cl-]. [Pd+2]. InChI=1S/2C18H15P. 2ClH. Pd/c2*1-4-10-16 (11-5-1) 19 (17-12-6-2-7-13-17) 18-14-8-3-9-15-18; ; ; /h2*1-15H; 2*1H; /q; ; ; ; +2/p-2. YNHIGQDRGKUECZ-UHFFFAOYSA-L. |  |
| Bis(triphenylphosphine)palladium(II) Dichloride | Precatalyst for the carbonylative cyclization of malonate derivatives. Catalyst used in the double allylation of activated olefins. Precatalyst for the three-component preparation of 3-arylidene- (or 3-alkenylidene) tetrahydrofurans. Precatalyst for the homocoupling of terminal alkynes. Precatalyst in the cross-coupling of alkynylsilanols and aryl halides. Catalyst for direct Pd-catalyzed alkynylation of N-fused heterocycles. Catalyst for a tandem Heck reaction/C-H functionalization. Catalyst for direct arylation of tautomerizable heterocycles. Group: Palladium series catalysts. Alternative Names: TRANS-BIS-(TRIPHENYLPHOSPHINE)PALLADIUM DICHLORIDE; 13965-03-2; 28966-81-6; AC1L36TY; SC-01002; LS-192238; bis(triphenylphosphine) palladiuml(II) dichloride; bis(triphenylphosphine) palladium (II) chloride; FC0823; EINECS 237-744-2. CAS No. 13965-03-2. Molecular formula: C36H30Cl2P2Pd. Mole weight: 701.904g/mol. IUPACName: palladium(2+); triphenylphosphane; dichloride. Canonical SMILES: C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. C1=CC=C (C=C1)P (C2=CC=CC=C2)C3=CC=CC=C3. [Cl-]. [Cl-]. [Pd+2]. ECNumber: 237-744-2. Catalog: ACM13965032. | |
| Boc-aminooxy-amide-PEG4-propargyl | CuAAC & Thiol-Yne & Spontaneous Amino-Yne Click Reaction. Group: Terminal alkynes. CAS No. 2253965-01-2. Molecular formula: C18H32N2O8. Mole weight: 404.46. IUPACName: tert-Butyl N- [2-oxo-2- [2- [2- [2- (2-prop-2-ynoxyethoxy) ethoxy] ethoxy] ethylamino] ethoxy] carbamate. Canonical SMILES: CC (C) (C)OC (=O)NOCC (=O)NCCOCCOCCOCCOCC#C. Catalog: CCR2253965012. | |
Our database is helping our users find suppliers everyday.
