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| Product | Description | |
|---|---|---|
| Chloro[(1,1'-biphenyl-2-yl)di-tert-butylphosphine]gold(I) | Highly active gold catalyst for the intramolecular exohydrofunctionalization of allenes. Catalyst used for the hydroarylation of allenes. Catalyst used for the intramolecular cyclization of monopropargyl triols. Synthesis of pyrroles via a gold-catalyzed cascade reaction. Gold-catalyzed carboalkoxylations of 2-ethynylbenzyl ethers. Gold-catalyzed annulations of allenes with N-hydroxy anilines. Group: Gold series of catalysts. Alternative Names: SC10751; JohnPhos AuCl; [[1,1 inverted exclamation marka-Biphenyl]-2-ylbis(t-butylphosphine]chlorogold; AKOS024259177; Chloro[(1,1'-biphenyl-2-yl)di-tert-butylphosphine]gold(I), 98%; KS-000019BH; TRA0069872; Chloro[2-(di-t-butylphosphino)biphenyl]gold(I). CAS No. 854045-93-5. Molecular formula: C20H27AuClP. Mole weight: 530.826g/mol. IUPACName: chlorogold;ditert-butyl-(2-phenylphenyl)phosphane. Canonical SMILES: CC (C) (C)P (C1=CC=CC=C1C2=CC=CC=C2)C (C) (C)C. Cl[Au]. Catalog: ACM854045935. |  |
| Chloro[(1,2,3-H)propenyl][di-tert-butylphenylphosphine]palladium(II) | Heterocyclic Organic Compound. Alternative Names: PdClAllyl(Amphos), Allyl (chloro) [di-tert-butyl (4-dimethylaminophenyl) phosphine]palladium (II) , 1235509-04-2. CAS No. 1235509-04-2. Molecular formula: C19H33ClNPPd. Mole weight: 448.318782 [g/mol]. Purity: 0.96. IUPACName: chloropalladium(1+);1-(4-ditert-butylphosphanylphenyl)-N-methylmethanamine;prop-1-ene. Catalog: ACM1235509042. | |
| Chloro[[(1, 2-η )-phenyl]diphenylphosphine-κ P](triphenylphosphine)rhodium | Rhodium Complexes. CAS No. 1095062-41-1. Molecular formula: C36H30ClP2Rh. Mole weight: 662.93. Purity: 0.98. Catalog: ACM1095062411. | |
| Chloro[1,3-bis(2,4,6-trimethylphenyl)2H-imidazol-2-ylidene]gold(I), 98% | Catalyst for the rearrangement of alkynyl sulfoxides to benzothiepinones Catalyst for the rearrangement of homopropargylic ethers to α,β-unsaturated carbonyl compounds Catalyst for oxidative cyclopropanation of N-Allylynamides to 3-aza-bicyclo[3.1.0]-hexan-2-one derivatives Catalyst for oxidative rearrangement of homopropargylic ethers to cyclobutanones. Group: Gold series of catalysts. Alternative Names: 1,3-Bis(2,4,6-trimethylphenyl)imidazol-2-ylidene gold(I) chloride; Chloro[1,3-Bis(Mesityl)Imidazole-2-Ylidene]Gold(I); Chloro[1,3-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene]gold(I); C21H24AuClN2; Chloro[1,3-bis(2,4,6-trimethylphenyl)2H-imidazol-2-ylidene]gold(I); AuCl(IMes); Chloro(1,3-dimesityl-1H-imidazol-2(3H)-ylidene)aurate(I); 3213AC. CAS No. 852445-81-9. Molecular formula: C21H24AuClN2. Mole weight: 536.854g/mol. IUPACName: [1,3-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene]-chlorogold. Canonical SMILES: CC1=CC (=C (C (=C1)C)N2C=CN (C2=[Au]Cl)C3=C (C=C (C=C3C)C)C)C. Catalog: ACM852445819. | |
| Chloro[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidene]gold(I), 98% | Catalyst for the carboheterofunctionalization of alkenes with arylboronic acids Catalyst for the synthesis of 1-substituted benzo[b][1,4]diazepines. Group: Gold catalysts. Alternative Names: MFCD29037185;Chloro[1,3-bis(2,4,6-trimethylphenyl)-4,5-dihydroimidazol-2-ylidene]gold(I);852445-82-0. CAS No. 852445-82-0. Molecular formula: C21H26AuClN2. Mole weight: 538.87g/mol. IUPACName: [1,3-bis(2,4,6-trimethylphenyl)imidazolidin-2-ylidene]-chlorogold. Canonical SMILES: CC1=CC (=C (C (=C1)C)N2CCN (C2=[Au]Cl)C3=C (C=C (C=C3C)C)C)C. Catalog: ACM852445820. | |
| Chloro{1,3-bis[2,6-bis(1-methylethyl)phenyl]-1,3-dihydro-4,5-dimethyl-2H-imidazol-2-ylidene}gold(I), 98% IPrMeAuCl | Gold Catalysts. Alternative Names: 1192141-66-4;Chloro{1,3-bis[2,6-bis(1-methylethyl)phenyl]-1,3-dihydro-4,5-dimethyl-2H-imidazol-2-ylidene}gold(I), 98% IPrMeAuCl. CAS No. 1192141-66-4. Molecular formula: C29H41AuClN2-. Mole weight: 650.078g/mol. IUPACName: 1,3-bis[2,6-di(propan-2-yl)phenyl]-4,5-dimethyl-2H-imidazol-2-ide;chlorogold. Canonical SMILES: CC1=C (N ([CH-]N1C2=C (C=CC=C2C (C)C)C (C)C)C3=C (C=CC=C3C (C)C)C (C)C)C. Cl[Au]. Catalog: ACM1192141664. | |
| Chloro{1,3-bis[2,6-di-i-propylphenyl]-4,5-dihydroimidazol-2-ylidene}gold(I), 98% SIPrAuCl | Catalyst for the rearrangement of allylic acetates. Group: Gold catalysts. Alternative Names: 852445-84-2; Chloro{1, 3-bis[2, 6-bis(1-methylethyl)phenyl]-4, 5-dihydroimidazol-2-ylidene}gold(I); SIPrAuCl; MFCD29037186; Chloro{1, 3-bis[2, 6-bis(1-methylethyl)phenyl]}-4, 5-dihydroimidazol-2-ylidene]gold(I). CAS No. 852445-84-2. Molecular formula: C27H38AuClN2. Mole weight: 623.032g/mol. IUPACName: [1,3-bis[2,6-di(propan-2-yl)phenyl]imidazolidin-2-ylidene]-chlorogold. Canonical SMILES: CC (C)C1=C (C (=CC=C1)C (C)C)N2CCN (C2=[Au]Cl)C3=C (C=CC=C3C (C)C)C (C)C. Catalog: ACM852445842. | |
| Chloro[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](1-tert-butyl-1H-inden-1-yl)palladium(II) | Amination→Buchwald-Hartwig Aminaton; Cross Coupling Reactions with Arenes→Suzuki-Miyaura Coupling Reaction. Group: Catalysts for pharmaceutical. CAS No. 1779569-04-8. Molecular formula: C40H51ClN2Pd. Mole weight: 701.71. Purity: Metal purity 99.95. Catalog: ACM1779569048. | |
| Chloro[[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](acetanilide)palladium(II)] | Heterocyclic Organic Compound. Alternative Names: [1,3-Bis[2,6-di(propan-2-yl)phenyl]imidazol-2-ylidene]palladium;N-phenylacetamide;chloride. CAS No. 1228009-69-5. Molecular formula: C35H44ClN3OPd. Mole weight: 664.6. Purity: 0.98. IUPACName: [1,3-bis[2,6-di(propan-2-yl)phenyl]imidazol-2-ylidene]palladium;N-phenylacetamide;chloride. Canonical SMILES: CC (C)C1=C (C (=CC=C1)C (C)C)N2C=CN (C2=[Pd])C3=C (C=CC=C3C (C)C)C (C)C. CC (=O)NC1=CC=CC=[C-]1. [Cl-]. Catalog: ACM1228009695-1. | |
| Chloro[1, 3-bis (2, 6-diisopropylphenyl) imidazol-2-ylidene]copper (I) | Chloro[1, 3-bis (2, 6-diisopropylphenyl) imidazol-2-ylidene]copper (I) . Group: Biochemicals. Grades: Highly Purified. CAS No. 578743-87-0. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. US Biological Life Sciences. |  Worldwide |
| Chloro[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]copper(I) | Catalyst for the aziridination of olefins. Mild catalyst, superior to CuCl, in the methylenetriphenylphosphorane methyleneation of aldehydes and ketones. Copper(I) catalyzed alkylation of aryl and alkenylsilanes. Copper-catalyzed formal methylative and hydrogenative carboxylation of alkynes with carbon dioxide. Regioselective copper-catalyzed carboxylation of allylboronates with carbon dioxide. Carboxylation of organoboronic esters with potassium methyl carbonate under copper catalysis. Catalytic anti-Markovnikov hydrobromination of alkynes. Copper-catalyzed borylative cross-coupling of allenes and imines. Group: Heterocyclic organic compound. CAS No. 578743-87-0. Molecular formula: C27H36ClCuN2. Mole weight: 487.6. Purity: >98.0%(T). IUPACName: Chloro[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene]copper(I). Catalog: ACM578743870. | |
| Chloro[[1,3-bis(2,6-diisopropylphenyl)imidazol-2-ylidene](N,N-dimethyl-3,5-dimethoxybenzylamine)palladium(II)] | Heterocyclic Organic Compound. Alternative Names: SingaCycle(TM)-A2. CAS No. 1093348-08-3. Molecular formula: C38H52ClN3O2Pd. Mole weight: 724.71. Purity: >98.0%(T). IUPACName: [1,3-bis[2,6-di(propan-2-yl)phenyl]imidazol-2-ylidene]palladium;1-(3,5-dimethoxybenzene-6-id-1-yl)-N,N-dimethylmethanamine;chloride. Canonical SMILES: CC (C)C1=C (C (=CC=C1)C (C)C)N2C=CN (C2=[Pd])C3=C (C=CC=C3C (C)C)C (C)C. CN (C)CC1=[C-]C (=CC (=C1)OC)OC. [Cl-]. Catalog: ACM1093348083. | |
| Chloro[1, 3-bis (2, 6-diisopropylphenyl) imidazol-2-ylidene]silver | Chloro[1, 3-bis (2, 6-diisopropylphenyl) imidazol-2-ylidene]silver. Group: Biochemicals. Grades: Highly Purified. CAS No. 873297-19-9. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. US Biological Life Sciences. | Worldwide |
| Chloro[1,3-bis(adamantyl)2H-imidazol-2-ylidene]gold(I), 98% | Catalyst for the rearrangement of allylic acetates. Group: Gold catalysts. Alternative Names: SCHEMBL2800749; MFCD29037189; Chloro[1, 3-bis(adamantyl)2H-imidazol-2-ylidene]gold(I); 852445-88-6. CAS No. 852445-88-6. Molecular formula: C23H32AuClN2. Mole weight: 568.94g/mol. IUPACName: [1,3-bis(1-adamantyl)imidazol-2-ylidene]-chlorogold. Canonical SMILES: C1C2CC3CC1CC (C2) (C3)N4C=CN (C4=[Au]Cl)C56CC7CC (C5)CC (C7)C6. Catalog: ACM852445886. | |
| Chloro[1,3-bis(t-butyl)-2H-imidazol-2-ylidene]gold(I), 98% | Catalyst for the rearrangement of allylic acetates Catalyst for the α-allylation of enals and enones with alcohols. Group: Gold catalysts. Alternative Names: MFCD29037187;Chloro[1,3-bis(1,1'-dimethylethyl)2H-imidazol-2-ylidene]gold(I);839722-07-5. CAS No. 839722-07-5. Molecular formula: C11H20AuClN2. Mole weight: 412.712g/mol. IUPACName: chloro-(1,3-ditert-butylimidazol-2-ylidene)gold. Canonical SMILES: CC(C)(C)N1C=CN(C1=[Au]Cl)C(C)(C)C. Catalog: ACM839722075. | |
| Chloro(1,3-dimesitylimidazol-2-ylidene)copper(I) | Chloro(1,3-dimesitylimidazol-2-ylidene)copper(I). Group: Biochemicals. Alternative Names: [1, 3-Bis (2, 4, 6-trimethylphenyl) imidazol-2-ylidene]chlorocopper (I) . Grades: Highly Purified. CAS No. 873779-78-3. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. US Biological Life Sciences. | Worldwide |
| Chloro[(1,3-dimesitylimidazol-2-ylidene)(N,N-dimethylbenzylamine)palladium(II)] | Heterocyclic Organic Compound. Alternative Names: [1,3-Bis(2,4,6-trimethylphenyl)imidazol-2-ylidene]palladium;N,N-dimethyl-1-phenylmethanamine;chloride. CAS No. 1058661-78-1. Molecular formula: C30H36ClN3Pd. Mole weight: 580.5. Appearance: Powder. Purity: 98%+. IUPACName: [1,3-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene]palladium;N,N-dimethyl-1-phenylmethanamine;chloride. Canonical SMILES: CC1=CC (=C (C (=C1)C)N2C=CN (C2=[Pd])C3=C (C=C (C=C3C)C)C)C. CN (C)CC1=CC=CC=[C-]1. [Cl-]. Catalog: ACM1058661781-1. | |
| Chloro(1,5-cyclooctadiene)(1,10-phenanthroline)iridium(I) THF adduct, min. 98% | Catalyst used in the C-H borylation of N-Boc-indoles. Group: Iridium catalysts. CAS No. 41396-69-4. Molecular formula: C24H28ClIrNO. Mole weight: 516.05. Catalog: ACM41396694. | |
| Chloro(1,5-cyclooctadiene)[4,5-dimethyl-1,3-bis(2,4,6-trimethylphenyl)imidazol-2-ylidene] iridium(I), min. 98% | Iridium Catalysts. CAS No. 1118917-09-1. Molecular formula: C31H40ClIrN2. Mole weight: 668.33. Catalog: ACM1118917091. | |
| Chloro(1,5-cyclooctadiene)iridium(I) dimer | 1. Precursor to catalysts for the asymmetric hydrogenation of tri- and tetrasubstituted olefins. 2. Precursor to catalyst for enantioselective reduction of imines. 3. Precursor to catalyst for allylic alkylation. 4. Precursor to catalyst for allylic amination and etherification. 5. Precursor to catalyst for the reaction of aroyl chlorides with internal alkynes to produce substituted naphthalenes and anthracenes. 6. Ir-catalyzed addition of acid chlorides to terminal alkynes. 7. Intramolecular hydroamination of unactivated alkenes with secondary alkyl- and arylamines. 8. Enantioselective [2+2] cycloaddition. 9. Silyl-directed, Ir-catalyzed ortho-borylation of arenes. 10. Ir-catalyzed cross-coupling of styrene derivatives with allylic carbonates. 11. Transfer hydrogenative C-C coupling. Group: Iridium series of catalysts. Alternative Names: Bis(1,5-cyclooctadiene)diiridium(I) dichloride. CAS No. 12112-67-3. Molecular formula: C16H24Cl2Ir2. Mole weight: 671.71. Appearance: Red brown powder. Purity: 0.99. IUPACName: (1Z,5Z)-cycloocta-1,5-diene;iridium;dichloride. Canonical SMILES: C1CC=CCCC=C1. C1CC=CCCC=C1. [Cl-]. [Cl-]. [Ir]. [Ir]. ECNumber: 235-170-7. Catalog: ACM12112673-4. | |
| Chloro(1,5-cyclooctadiene)rhodium(I) dimer | Catalyst for coupling 1,3-dienes with activate methylene compounds. Rhodium source for various asymmetric hydrogenation systems and asymmetric hydrosilylation of ketones. Rhodium source for asymmetric reductive aldol reaction. Cis-hydroboration of terminal alkynes. Rhodium source for [5 + 2] additions. Highly enantioselective for [2+2+2] carbocyclization reactions. Enantioselective hydroboration of cyclopropenes. Group: Rhodium series of catalysts. Alternative Names: Bis(cycloocta-1,5-diene)dichlorodirhodium. CAS No. 12092-47-6. Molecular formula: C16H24Cl2Rh2. Mole weight: 493.08. Appearance: Orange yellow powder. Purity: 0.98. IUPACName: (1Z,5Z)-cycloocta-1,5-diene;rhodium;dichloride. Canonical SMILES: C1CC=CCCC=C1. C1CC=CCCC=C1. [Cl-]. [Cl-]. [Rh]. [Rh]. ECNumber: 235-157-6. Catalog: ACM12092476-2. | |
| Chloro(1,5-cyclooctadiene)rhodium(I) dimer | Chloro(1,5-cyclooctadiene)rhodium(I) dimer. Uses: Catalyst for coupling 1,3-dienes with activate methylene compounds. rhodium source for various asymmetric hydrogenation systems and asymmetric hydrosilylation of ketones. rhodium source for asymmetric reductive aldol reaction. cis-hydroboration of terminal alkynes. rhodium source for [5 + 2] additions. highly enantioselective for [2+2+2] carbocyclization reactions. enantioselective hydroboration of cyclopropenes. Group: Salt. Alternative Names: Bis(cycloocta-1,5-diene)dichlorodirhodium. CAS No. 12092-47-6. Product ID: (1Z,5Z)-cycloocta-1,5-diene; rhodium; dichloride. Molecular formula: 493.08. Mole weight: C16H24Cl2Rh2. C1CC=CCCC=C1. C1CC=CCCC=C1. [Cl-]. [Cl-]. [Rh]. [Rh]. InChI=1S/2C8H12. 2ClH. 2Rh/c2*1-2-4-6-8-7-5-3-1; /h2*1-2, 7-8H, 3-6H2; 2*1H; /p-2/b2*2-1-, 8-7-. PDJQCHVMABBNQW-MIXQCLKLSA-L. 98%. |  |
| Chloro (1, 5-cyclooctadiene)rhodium (I) Dimer | Chloro (1, 5-cyclooctadiene)rhodium (I) Dimer is used in the synthesis of metal ligands for used in catalysis reactions. Group: Biochemicals. Alternative Names: (1, 5-Cyclooctadiene) ?Rhodium Chloride Dimer; (1,5-Cyclooctadiene) Rhodium(I) Chloride Dimer; (η 4-1, 5-Cyclooctadiene) ?Rhodium Chloride Dimer; Bis ( (1, ?5-cyclooctadiene)? (Chloro)?Rhodium); Bis ( (μ -chloro) ? (η 4-1, 5-Cyclooctadiene) ?Rhodium) ; Bis (1, 5-cyclooctadiene) ?Dirhodium Dichloride; Bis (chloro (1, 5-cyclooctadiene) ?Rhodium) ; Bis (chloro (η 4-1, 5-cyclooctadiene) ?rhodium) ; Bis (cyclooctadiene) ?Dichlorodirhodium; Bis (cyclooctadienerhodium Chloride); Chlororhodium(1,5-cyclooctadiene) Dimer; Cyclooctadiene Rhodium Chloride Dimer; Di-μ -Chlorobis (1, 5-cyclooctadiene) ?Dirhodium; Di-μ -chlorobis (cyclooctadiene) Dirhodium; Di-μ -?chlorobis (η 4-?1, ?5-?cyclooctadiene) ?dirhodium; Di-μ -chlorobis (η 4-1, ?5-cyclooctadiene) ?Dirhodium (I) ; Di-μ -chlorobis [ (1, 2, 5, 6-η ) -1, 5-cyclooctadiene] ?Dirhodium; Di-μ -chlorobis[ (1, 5-cyclooctadiene) ?Rhodium]; Di-μ 2-chlorobis (1, 5-?cyclooctadiene) ?Dirhodium; Dichlorobis (1, 5-cyclooctadiene) ?Dirhodium; Dichlorobis (1, ?5-cyclooctadiene) ?Rhodium (I) ; Dichlorobis (cyclooctadiene) ?Dirhodium; Rhodium 1,5-?Cyclooctadiene chloride dimer; μ -Chloro (1, 5-cyclooctadiene) ?Rhodium (I) Dimer; Bis (1, 5-cyclooctadiene dirhodium (I) Chloride). Grades: Highly Purified. CAS No. 12092-47-6. Pack Sizes: 500mg. US Biological Life Sciences. | Worldwide |
| Chloro (1-phenylindenyl)bis (triphenylphosphine)ruthenium (II), min. 98% | Efficient, ruthenium-catalyzed S-S, S-Si, and S-B bond forming reactions. Chemoselective oxidation of secondary alcohols to ketones. Ruthenium complex used as an efficient transfer hydrogenation catalyst. Catalyst for the racemization of chiral alcohols. Group: Ruthenium catalysts. Alternative Names: MFCD23704804; Chloro (3-phenylindenyl)bis (triphenylphosphine)ruthenium (II); 1360949-97-8. CAS No. 1360949-97-8. Molecular formula: C51H41ClP2Ru. Mole weight: 852.357g/mol. IUPACName: chlororuthenium;1-phenylindene;triphenylphosphane. Canonical SMILES: C1=CC=C (C=C1) [C]2 [CH] [CH] [C]3 [C]2 [CH] [CH] [CH] [CH]3. 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 [Ru]. Catalog: ACM1360949978. | |
| Chloro{ (1R, 2R)-1, 2-diphenyl-1-[ (3- (η 6-phenyl)propyl)amino]-2- (methylsulfonylamido)}ruthenium (II) RuCl[(R,R)teth-MsDpen] | Catalyst used for asymmetric -transfer hydrogenation. Group: Ruthenium catalysts. CAS No. 1361415-88-4. Molecular formula: C24H27ClN2O2RuS. Mole weight: 544.07. Catalog: ACM1361415884. | |
| Chloro{ (1S, 2S)-1, 2-diphenyl-1-[ (3- (η 6-phenyl)propyl)amino]-2- (methylsulfonylamido)}ruthenium (II) RuCl[(S,S)teth-MsDpen] | Catalyst used for asymmetric -transfer hydrogenation. Group: Ruthenium catalysts. Alternative Names: MFCD22988933;1437326-26-5;Chloro[(S, S)-N1-methylsulfonyl-1, 2-diphenyl-N2-(3-phenylpropyl)-1, 2-ethanediamine]ruthenium(II);[(S, S)-Teth-MsDPEN-RuCl], Ru 18. 5%; Chloro{ (1S, 2S)-1, 2-diphenyl-1-[ (3- (6-phenyl)propyl)amino]-2- (methylsulfonylamido)}ruthenium (II) RuCl[(S,S)2teth-MsDpen]. CAS No. 1437326-26-5. Molecular formula: C24H27ClN2O2RuS. Mole weight: 544.072g/mol. IUPACName: chlororuthenium (1+) ; [ (1S, 2S) -1, 2-diphenyl-2- (3-phenylpropylamino) ethyl]-methylsulfonylazanide. Canonical SMILES: CS (=O) (=O)[N-]C (C1=CC=CC=C1)C (C2=CC=CC=C2)NCCCC3=CC=CC=C3. Cl[Ru+]. Catalog: ACM1437326265. | |
| Chloro[(1S, 2S)-N-(2', 6'-dimethylbenzylsulfonyl)-1, 2-diphenylethanediamine](p-cymene)ruthenium(II) | Ruthenium Complexes. Alternative Names: [ (1S, 2S) -2-Amino-1, 2-diphenylethyl]-[ (2, 6-dimethylphenyl) methylsulfonyl]azanide; chlororuthenium (1+) ; 1-methyl-4-propan-2-ylbenzene. CAS No. 1251757-36-4. Molecular formula: C33H39ClN2O2RuS. Mole weight: 664.3. Purity: 0.98. Canonical SMILES: CC1=CC=C (C=C1)C (C)C. CC1=C (C (=CC=C1)C)CS (=O) (=O)[N-]C (C2=CC=CC=C2)C (C3=CC=CC=C3)N. Cl[Ru+]. Catalog: ACM1251757364. | |
| Chloro (1-t-butylindenyl)[2- (dicyclohexylphosphino)-2', 4', 6'-tri-i-propyl-1, 1'-biphenyl]palladium (II) | Catalyst used in the α-arylation of ketones. Catalyst used in the Suzuki cross-coupling of aryl chlorides with boronic acid-substituted benzofurans. Group: Palladium catalysts. CAS No. 1779569-06-0. Molecular formula: C46H64ClPPd. Mole weight: 789.85. Appearance: Orange powder. Catalog: ACM1779569060-1. | |
| Chloro (1-t-butylindenyl)[2- (dicyclohexylphosphino)-2', 6'-di-i-propoxy-1, 1'-biphenyl]palladium (II) | Catalyst used in the Buchwald-Hartwig cross-coupling of substituted aryl chlorides with secondary amines. Group: Palladium catalysts. CAS No. 1779569-08-2. Molecular formula: C43H58ClO2PPd. Mole weight: 779.77. Appearance: Orange powder. Catalog: ACM1779569082-1. | |
| Chloro (1-t-butylindenyl)[2- (dicyclohexylphosphino)-2', 6'-dimethoxy-1, 1'-biphenyl]palladium (II) | Catalyst used in the Suzuki cross-coupling of 3-chloroindazole or 3-chlorobenzimidazole with arylboronic acids. Group: Palladium catalysts. CAS No. 1779569-07-1. Molecular formula: C39H50ClO2PPd. Mole weight: 723.66. Appearance: Orange powder. Purity: 0.98. Catalog: ACM1779569071-1. | |
| Chloro(1-tert-butyl-1H-inden-1-yl)(tri-tert-butylphosphine)palladium(II) | Amination→Buchwald-Hartwig Aminaton; Cross Coupling Reactions with Arenes→Suzuki-Miyaura Coupling Reaction. Group: Catalysts for pharmaceuticalamination. CAS No. 1779569-15-1. Molecular formula: C25H42ClPPd. Mole weight: 515.45. Catalog: ACM1779569151-1. | |
| Chloro{2-[1-(N-methoxy)iminoethyl]phenyl}{[1,3-bis(2,6-di-i-propylphenyl]imidzole-2-ylidene}palladium(II) | Extremely active palladium catalyst for Suzuki-Miyaura coupling of aryl chlorides. Group: Palladium catalysts. CAS No. 1511859-41-8. Molecular formula: C36H46ClN3OPd. Mole weight: 678.64. Appearance: Pale yellow powder. Catalog: ACM1511859418-1. | |
| Chloro{2-[(1-(N-phenyl)iminoethyl]phenyl}{[1,3-bis(2,6-di-i-propylphenyl]imidzole-2-ylidene}palladium(II) | Extremely active palladium catalyst for Suzuki-Miyaura coupling of aryl chlorides. Group: Palladium catalysts. CAS No. 1905460-13-0. Molecular formula: C41H48ClN3Pd. Mole weight: 724.71. Appearance: Pale yellow powder. Purity: 0.97. Catalog: ACM1905460130-1. | |
| Chloro(2,2'-bipyridine)(4'-carboxy-2,2',2''-terpyridine)ruthenium(1+) hydrochloride | Ruthenium Complexes. CAS No. 1220636-19-0. Molecular formula: C26H19Cl2N5O2Ru. Mole weight: 620.47. Catalog: ACM1220636190. | |
| Chloro 2,3,5-tri-O-p-chlorobenzoyl-beta-D-ribofuranoside | Heterocyclic Organic Compound. CAS No. 125598-74-5. Molecular formula: C26H18Cl4O7. Catalog: ACM125598745. | |
| Chloro 2,3,5-Tri-O-p-chlorobenzoyl-β-D-ribofuranoside | Chloro 2,3,5-Tri-O-p-chlorobenzoyl-β-D-ribofuranoside is a compound useful in organic synthesis. Synonyms: β-D-Ribofuranosyl Chloride Tris(4-chlorobenzoate). Grades: 98%. Molecular formula: C26H18Cl4O7. Mole weight: 584.23. |  |
| Chloro-(2'-chloro)trityl Polystyrene, Type1 | A very acid-sensitive resin is suitable for the synthesis of protected peptide fragments by the Fmoc strategy. In particular suitable for the preparation of C-terminal prolyl and cysteinyl peptides. Cleavage from this resin is achieved by using 1-95% TFA in CH2Cl2 (containing 8% triisopropylsilane), AcOH/CF3OH/CH2Cl2, 0.5% TFA or hexafluoroisopropanol. Uses: Recently, this resin has been used in cyclization reactions under heck reaction conditions, the solid phase synthesis of b-peptides via the arndt-eistert homologation of fmoc-protected amino acid diazoketones and in mannich reactions of alkynes, secondary amines and aldehydes in the presence of a copper (I) salt leading to the corresponding aminomethylalkynyl adducts. this resin can also be used in fmoc peptide synthesis. 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 these conditions. Group: Chloro-(2-chloro)trityl polystyrene resins. Pack Sizes: 5g, 25g, 100g. | |
| Chloro-(2'-chloro)trityl Polystyrene, Type2 | A very acid-sensitive resin is suitable for the synthesis of protected peptide fragments by the Fmoc strategy. In particular suitable for the preparation of C-terminal prolyl and cysteinyl peptides. Cleavage from this resin is achieved by using 1-95% TFA in CH2Cl2 (containing 8% triisopropylsilane), AcOH/CF3OH/CH2Cl2, 0.5% TFA or hexafluoroisopropanol. Uses: Recently, this resin has been used in cyclization reactions under heck reaction conditions, the solid phase synthesis of b-peptides via the arndt-eistert homologation of fmoc-protected amino acid diazoketones and in mannich reactions of alkynes, secondary amines and aldehydes in the presence of a copper (I) salt leading to the corresponding aminomethylalkynyl adducts. this resin can also be used in fmoc peptide synthesis. 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 these conditions. Group: Chloro-(2-chloro)trityl polystyrene resins. Pack Sizes: 5g, 25g, 100g. | |
| Chloro-(2'-chloro)trityl Polystyrene, Type3 | A very acid-sensitive resin is suitable for the synthesis of protected peptide fragments by the Fmoc strategy. In particular suitable for the preparation of C-terminal prolyl and cysteinyl peptides. Cleavage from this resin is achieved by using 1-95% TFA in CH2Cl2 (containing 8% triisopropylsilane), AcOH/CF3OH/CH2Cl2, 0.5% TFA or hexafluoroisopropanol. Uses: Recently, this resin has been used in cyclization reactions under heck reaction conditions, the solid phase synthesis of b-peptides via the arndt-eistert homologation of fmoc-protected amino acid diazoketones and in mannich reactions of alkynes, secondary amines and aldehydes in the presence of a copper (I) salt leading to the corresponding aminomethylalkynyl adducts. this resin can also be used in fmoc peptide synthesis. 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 these conditions. Group: Chloro-(2-chloro)trityl polystyrene resins. Pack Sizes: 5g, 25g, 100g. | |
| Chloro[2-dicyclohexyl(2', 6';-diisopropoxybiphenyl)phosphine] gold(I) | Gold Catalysts. CAS No. 1261452-57-6. Mole weight: 699.05. Catalog: ACM1261452576. | |
| Chloro[2-dicyclohexyl(2', 6'-dimethoxybiphenyl)phosphine] gold(I) | Highly-efficient and regio-selective catalyst for the selective carbonyl migration in alkynyl-substituted indole-3-carboxamides. Catalyst used in the hydroarylation/aromatization of arene-diynes. Catalyst used in the selective hydration of substituted alkynes at room temperatures. Group: Gold catalysts. Alternative Names: MFCD21608486;Chloro(2-dicyclohexylphosphino-2',6'-dimethoxy-1,1'-biphenyl)gold(I);854045-95-7. CAS No. 854045-95-7. Molecular formula: C26H36AuClO2P+. Mole weight: 643.962g/mol. IUPACName: chlorogold;dicyclohexyl-[2-(2,6-dimethoxyphenyl)phenyl]phosphanium. Canonical SMILES: COC1=C (C (=CC=C1)OC)C2=CC=CC=C2[PH+] (C3CCCCC3)C4CCCCC4. Cl[Au]. Catalog: ACM854045957. | |
| Chloro(2-dicyclohexylphosphino-2',6'-di-i-propoxy-1,1'-biphenyl)[2-(2-aminoethylphenyl)]palladium(II), methyl-t-butylether adduct, min. 98% [RuPhos Palladacycle Gen. 1] | Catalyst used in the thermal dehydrogenative Diels-Alder reaction of styrenes. Catalyst used for the CN-cross coupling reactions of 3-halo-2-aminopyridines. Catalyst used for the domino reaction of two aryl iodides, involving two C-H functionizations. Group: Palladium series catalysts. Alternative Names: Chloro-(2-Dicyclohexylphosphino-2a 6a diisopropoxy-1,1a biphenyl)[2-(2-aminoethyl)phenyl]palladium(II) - methyl-t-butyl ether adduct (RuPhos Precatalyst 1st Gen); 1028206-60-1; Chloro-(2-Dicyclohexylphosphino-2 inverted exclamation marka,6 inverted exclamation marka-diisopropoxy-1,1 inverted exclamation marka-biphenyl)[2-(2-aminoethyl)phenyl]palladium(II) - methyl-t-butyl ether adduct; KS-0000005C. CAS No. 1028206-60-1. Molecular formula: C43H65ClNO3PPd. Mole weight: 816.841g/mol. IUPACName: chloropalladium(1+); dicyclohexyl-[2-[2, 6-di(propan-2-yloxy)phenyl]phenyl]phosphane; 2-methoxy-2-methylpropane; 2-phenylethanamine. Canonical SMILES: CC (C)OC1=C (C (=CC=C1)OC (C)C)C2=CC=CC=C2P (C3CCCCC3)C4CCCCC4. CC (C) (C)OC. C1=CC=C ([C-]=C1)CCN. Cl[Pd+]. Catalog: ACM1028206601. | |
| Chloro(2-dicyclohexylphosphino-2',6'-dimethoxy-1,1'-biphenyl)[2-(2-aminoethylphenyl)]palladium(II) methyl-t-butylether adduct, min. 98% [SPhos Palladacycle Gen. 1] | Palladium series catalysts. Alternative Names: SPhos Palladacycle. CAS No. 1028206-58-7. Molecular formula: C34H45ClNO2PPd. Mole weight: 672.57. Appearance: white to off-white powder or crystals. Catalog: ACM1028206587. | |
| Chloro[2-(dicyclohexylphosphino)-2'-(N,N-dimethylamino))-1,1'-biphenyl]gold(I), 98% | Catalyst used in the formation of a bisenamines from toluidine and phenylacetylene. Catalyst used for the intermolecular hydroamination of alkynes with amines. Catalyst used for the regio and stereoselective, intermolecular hydroalkylations of alkynes. Catalyst used in the synthesis of dihydroisocoumarins. Group: Gold catalysts. Alternative Names: MFCD21363040; Chloro[2-(dicyclohexylphosphino)-2'-(N, N-dimethylamino)biphenyl]gold(I); 1196707-11-5. CAS No. 1196707-11-5. Molecular formula: C26H37AuClNP+. Mole weight: 626.979g/mol. IUPACName: chlorogold; dicyclohexyl-[2-[2- (dimethylamino) phenyl]phenyl]phosphanium. Canonical SMILES: CN (C)C1=CC=CC=C1C2=CC=CC=C2[PH+] (C3CCCCC3)C4CCCCC4. Cl[Au]. Catalog: ACM1196707115. | |
| Chloro[2-(dicyclohexylphosphino)-3,6-dimethoxy-2',4',6'-tri-i-propyl-1,1'-biphenyl][2-(2-aminoethyl)phenyl]palladium(II), min. 98% [BrettPhos Palladacycle Gen. 1] | Catalyst for cross-coupling reactions using aryl mesylates with electron-deficient anilines. Catalyst for rapid C-N bond-forming processes at low catalyst loading. Cross-coupling of 3-Bromo-2-aminopyridine with primary amines. Group: Palladium series catalysts. Alternative Names: BrettPhos Palladacycle. CAS No. 1148148-01-9. Molecular formula: C43H63ClNO2PPd. Mole weight: 798.81. Appearance: white to off-white powder or crystals. Purity: 0.97. Catalog: ACM1148148019. | |
| Chloro(2-dicyclohexylphosphino-3,6-dimethoxy-2',4',6'-tri-i-propyl-1,1'-biphenyl)(2'-amino-1,1'-biphenyl-2-yl)palladium(II) | Chloro(2-dicyclohexylphosphino-3,6-dimethoxy-2',4',6'-tri-i-propyl-1,1'-biphenyl)(2'-amino-1,1'-biphenyl-2-yl)palladium(II). CAS No. 1451002-39-3. Product ID: PE-0336. Molecular formula: C47H63ClNO2PPd. Mole weight: 846.86 g/mol. Category: Catalysts. Product Keywords: Pharmaceutical Excipients; Catalysts; Chloro(2-dicyclohexylphosphino-3,6-dimethoxy-2',4',6'-tri-i-propyl-1,1'-biphenyl)(2'-amino-1,1'-biphenyl-2-yl)palladium(II); PE-0336; 1451002-39-3; C47H63ClNO2PPd; Chloro(2-dicyclohexylphosphino-3,6-diMethoxy-2',4',6'-tri-i-propyl-1,1'-biphenyl)(2'-aMino-1,1'-biphenyl-2-yl)palladiuM(II), Min. 98% [BrettPhos Palladacycle]; 1451002-39-3. Appearance: White powder. Purity: 0.98. Synonym(s): Chloro(2-dicyclohexylphosphino-3,6-diMethoxy-2',4',6'-tri-i-propyl-1,1'-biphenyl)(2'-aMino-1,1'-biphenyl-2-yl)palladiuM(II), Min. 98% [BrettPhos Palladacycle]. |  |
| Chloro(2-dicyclohexylphosphino-3,6-dimethoxy-2',4',6'-tri-i-propyl-1,1'-biphenyl)(2'-amino-1,1'-biphenyl-2-yl)palladium(II), min. 98% [BrettPhos Palladacycle Gen. 2] | Palladium precatalyst for fast Suzuki-Miyaura coupling reactions. Coupling of chloropyrazoles with boronic acis. Group: Palladium catalysts. Alternative Names: BrettPhos Palladacycle Gen. 2;MFCD22666410;1451002-39-3. CAS No. 1451002-39-3. Molecular formula: C47H63ClNO2PPd. Mole weight: 846.87g/mol. IUPACName: chloropalladium(1+);dicyclohexyl-[3,6-dimethoxy-2-[2,4,6-tri(propan-2-yl)phenyl]phenyl]phosphane;2-phenylaniline. Canonical SMILES: CC (C)C1=CC (=C (C (=C1)C (C)C)C2=C (C=CC (=C2P (C3CCCCC3)C4CCCCC4)OC)OC)C (C)C. C1=CC=C ([C-]=C1)C2=CC=CC=C2N. Cl[Pd+]. Catalog: ACM1451002393. | |
| Chloro(2-di-tert-butylphosphino-3,4,5,6-tetramethyl-2',4',6'-triisopropylbiphenyl)gold(I) | Gold Catalysts. CAS No. 1140907-91-0. Mole weight: 713.17. Catalog: ACM1140907910. | |
| Chloro(2-methylphenyl)(N,N,N',N'-tetramethyl-1,2-ethylenediamine)nickel(II), 99% (contains about 5% o-chlorotoluene) NiCl(o-tolyl)(TMEDA) | Air-Stable Nickel precatalyst for cross-coupling Precatalyst allowing various ligands to be used (monoand bidendate phosphines, diimines and NHCs). Group: Nickel catalysts. Alternative Names: Chloro(2-methylphenyl)(N, N, N, N-tetramethyl-1, 2-ethylenediamine)nickel(II); 1702744-45-3; [(TMEDA)Ni(o-tolyl)Cl]; F1905-8610. CAS No. 1702744-45-3. Molecular formula: C13H23ClN2Ni-. Mole weight: 301.484g/mol. IUPACName: chloronickel;methylbenzene;N, N, N', N'-tetramethylethane-1, 2-diamine. Canonical SMILES: CC1=CC=CC=[C-]1.CN(C)CCN(C)C.Cl[Ni]. Catalog: ACM1702744453. | |
| Chloro(4, 4'-dichloro-2, 2'-bipyridine)(2, 2', 2''-terpyridine)ruthenium(1+) monochloride | Ruthenium Complexes. CAS No. 1220636-15-6. Molecular formula: C25H17Cl4N5Ru. Mole weight: 645.35. Catalog: ACM1220636156. | |
| Chloro(4,4'-dichloro-2,2'-bipyridine)(4'-chloro-2,2',2''-terpyridine)ruthenium(1+) monochloride | Ruthenium Complexes. CAS No. 1220636-17-8. Molecular formula: C25H16Cl5N5Ru. Mole weight: 679.79. Catalog: ACM1220636178. | |
| Chloro(4,4'-dimethoxy-2,2'-bipyridine)(4'-methoxy-2,2',2''-terpyridine)ruthenium(1+) monochloride | Ruthenium Complexes. CAS No. 1220636-11-2. Molecular formula: C28H25Cl2N5O3Ru. Mole weight: 666.54. Catalog: ACM1220636112. | |
| Chloro(4-chlorophenyl)phenylmethane | Chloro(4-chlorophenyl)phenylmethane. CAS No: 134-83-8 |  Sarchem Laboratories New Jersey NJ |
| Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- [bis (4-fluorophenyl] phosphino] ferrocenyl] ethyldi-tert-butylphosphine] nickel (II) | Chloro (4-cyanophenyl) { (R) -1-[ (S) -2- (bis (4-fluorophenyl) phosphinoferrocenyl]ethyl (di-t-butylphosphine) }nickel (II) is used for: 1.Versatile air-stable low cost nickel catalyst alternative to palladium for carbon-carbon and carbonheteroatom cross-coupling reactions. 2.Used to react substituted aryl and heteroaryl halides and tosylates with ammonia to produce diverse aryl and heteroaryl amines. 3.Used in monoarylation experiments using commercially available ammonia gas, ammonium salts or ammonia stock solutions. 4.Catalyzes the coupling of aryl chlorides with gaseous amines in the form of their hydrochloride salts. Group: Nickel catalysts. CAS No. 2049086-37-3. Mole weight: 774.69. Catalog: ACM2049086373. | |
| Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- (dicyclohexylphosphino) ferrocenyl] ethyldicyclohexylphosphine] nickel (II) | Versatile air-stable low cost nickel catalyst alternative to palladium for carbon-carbon and carbonheteroatom cross-coupling reactions. Used to react substituted aryl and heteroaryl halides and tosylates with ammonia to produce diverse aryl and heteroaryl amines. Used in monoarylation experiments using commercially available ammonia gas, ammonium salts or ammonia stock solutions. Catalyzes the coupling of aryl chlorides with gaseous amines in the form of their hydrochloride salts. Group: Nickel catalysts. CAS No. 2049086-35-1. Mole weight: 802.88. Catalog: ACM2049086351. | |
| Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- (dicyclohexylphosphino) ferrocenyl] ethyldiphenylphosphine] nickel (II) | Chloro (4-cyanophenyl) { (R) -1-[ (S) -2- (dicyclohexylphosphino) ferrocenyl]ethyl (diphenylphosphine)}nickel(II) is useful in these fields: Versatile air-stable low cost nickel catalyst alternative to palladium for carbon-carbon and carbonheteroatom cross-coupling reactions. Used to react substituted aryl and heteroaryl halides and tosylates with ammonia to produce diverse aryl and heteroaryl amines Used in monoarylation experiments using commercially available ammonia gas, ammonium salts or ammonia stock solutions Catalyzes the coupling of aryl chlorides with gaseous amines in the form of their hydrochloride salts. Group: Nickel catalysts. CAS No. 2049086-36-2. Mole weight: 790.79. Catalog: ACM2049086362. | |
| Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- (diphenylphosphino) ferrocenyl] ethylditertbutylphosphine] nickel (II) | Chloro (4-cyanophenyl) [ (R) -1- [ (S) -2- (diphenylphosphino) ferrocenyl] ethylditertbutylphosphine] nickel (II) has the following various uses:1.Versatile, air-stable, low cost nickel catalyst alternative to palladium for carbon-carbon and carbonheteroatom cross-coupling reactions. 2.Used to react substituted aryl and heteroaryl halides and tosylates with ammonia to produce diverse aryl and heteroaryl amines. 3.Used in monoarylation experiments using commercially available ammonia gas, ammonium salts or ammonia stock solutions Catalyzes the coupling of aryl chlorides with gaseous amines in the form of their hydrochloride salts. Group: Nickel catalysts. CAS No. 2049086-34-0. Mole weight: 738.71. Catalog: ACM2049086340. | |
| Chloro[(4-methylphenyl)diphenylphosphine]gold | Gold Complexes. Alternative Names: Chloro-(triphenyl-lambda5-phosphanylidene)gold. CAS No. 107198-68-5. Molecular formula: C18H15AuClP. Mole weight: 494.7. Purity: 0.98. Canonical SMILES: C1=CC=C (C=C1)P (=[Au]Cl) (C2=CC=CC=C2)C3=CC=CC=C3. Catalog: ACM107198685. | |
| Chloro-5-fluoro-pyridine-3-carbaldehyde | Chloro-5-fluoro-pyridine-3-carbaldehyde. Group: Biochemicals. Grades: Highly Purified. CAS No. 1060802-34-7. Pack Sizes: 500mg, 1g, 2g, 5g, 10g. US Biological Life Sciences. | Worldwide |
| Chloro (5-methoxy-2-{1-[ (4-methoxyphenyl)imino-N]ethyl}phenyl-C) (1, 2, 3, 4, 5-pentamethylcyclopentadienyl)iridium (III) | A versatile catalyst for reductive amination by hydrogen transfer. Acceptorless dehydrogenation of nitrogen heterocycles with a versatile iridium catalyst. Group: Iridium catalysts. CAS No. 1258964-48-5. Mole weight: 617.2. Catalog: ACM1258964485. | |
| Chloroacetaldehyde Aldolase (Crude Enzyme) | This product with the indicated enzyme activity was briefly purified from engineered E. coli. Group: Enzymes. Enzyme Commission Number: EC 4.1.2.X. Activity: Undetermined. Appearance: Clear to translucent yellow solution. Storage: at -20 °C or lower, for at least 1 month. Source: E. coli. Chloroacetaldehyde Aldolase. Pack: 100ml. Cat No: NATE-1849. |  |
| Chloroacetaldehyde Sodium Bisulfite, 95% | Chloroacetaldehyde Sodium Bisulfite, 95%. Group: other glass and ceramic materials. CAS No. 13064-50-1. Product ID: sodium; 2-chloro-1-hydroxyethanesulfonate. Molecular formula: 182.56g/mol. Mole weight: C2H4ClNaO4S. C(C(O)S(=O)(=O)[O-])Cl.[Na+]. InChI=1S/C2H5ClO4S.Na/c3-1-2(4)8(5, 6)7;/h2, 4H, 1H2, (H, 5, 6, 7);/q;+1/p-1. FOSIEWVVVRVFJH-UHFFFAOYSA-M. | |
| Chloroacetamide | Chloroacetamide. Uses: For analytical and research use. Group: Impurity standards. CAS No. 79-07-2. Molecular Formula: C2H4ClNO. Mole Weight: 93.51. Catalog: APB79072. |  |
| Chloroacetamide-d4 | Heterocyclic Organic Compound. Alternative Names: CHLOROACETAMIDE-D4. CAS No. 122775-20-6. Molecular formula: C2ClD4NO. Mole weight: 97.54. Appearance: White Solid. Purity: 99 atom % D. Catalog: ACM122775206. | |
| Chloroacetic acid | 100g Pack Size. Group: Building Blocks, Organics. Formula: C2H3ClO2. CAS No. 79-11-8. Prepack ID 38682736-100g. Molecular Weight 94.5. See USA prepack pricing. |  |
| Chloroacetic Acid | Chloroacetic Acid. CAS No. 79-11-8. Molecular Formula CH2ClCOOH. Chemical Reagents |  Cater Chemicals Corp. Illinois IL |
| Chloroacetic Acid | Chloroacetic Acid is used to detect hydrated electron (e-aq) generated in p-benzoquinone/UV process. Group: Biochemicals. Grades: Highly Purified. CAS No. 79-11-8. Pack Sizes: 1g, 10g, 250g, 500g. Molecular Formula: C?H?ClO?. US Biological Life Sciences. | Worldwide |
| Chloroacetic Acid-13C2 | Chloroacetic Acid-13C2. Group: Biochemicals. Alternative Names: Monochloroacetic Acid-13C2; NSC 142-13C2; NSC 42970-13C2. Grades: Highly Purified. Pack Sizes: 10mg. US Biological Life Sciences. | Worldwide |
| Chloroacetone stab. with 0.1% epoxidized soybean oil | 100g Pack Size. Group: Building Blocks, Organics. Formula: C3H5ClO. CAS No. 78-95-5. Prepack ID 90026858-100g. Molecular Weight 92.52. See USA prepack pricing. | |
| Chloroacetonitrile | 100g Pack Size. Group: Building Blocks, Organics. Formula: C2H2ClN. CAS No. 107-14-2. Prepack ID 36098756-100g. Molecular Weight 75.5. See USA prepack pricing. | |
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