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Brc1cnc(nc1)C
Pyrimidine, 5-bromo-2-methyl-
CCCP1(=O)OP(=O)(CCC)OP(=O)(O1)CCC
1,3,5,2,4,6-Trioxatriphosphorinane, 2,4,6-tripropyl-, 2,4,6-trioxide
CC1(C)OB(OC1(C)C)B1OC(C(O1)(C)C)(C)C
2,2'-Bi-1,3,2-dioxaborolane, 4,4,4',4',5,5,5',5'-octamethyl-
O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.O=C(C=Cc1ccccc1)C=Cc1ccccc1.[Pd].[Pd]
Tris(dibenzylideneacetone)dipalladium
C1CCC(CC1)P(C1CCCCC1)C1CCCCC1.Cc1cc(C)c(c(c1)C)N1CCN(C1=[Ru](=Cc1ccccc1)(Cl)Cl)c1c(C)cc(cc1C)C
Ruthenium,[1,3-bis(2,4,6-trimethylphenyl)-2-imidazolidinylidene]dichloro(phenylmethylene)(tricyclohexylphosphine)-, (SP-5-41)-

pyridine;trichlorogold

c1cccnc1.Cl[Au](Cl)Cl Request for Quotation
Chemical Name: pyridine;trichlorogold
CAS Number: 14911-01-4
Product Number: AG001LF1(AGN-PC-0JR2HJ)
Synonyms:
MDL No:
Molecular Formula: C5H5AuCl3N
Molecular Weight: 382.42545

Identification/Properties

Safety Information

GHS Pictogram:
Signal Word:
Warning
UN#:
-
Hazard Statements:
H315-H319-H335
Precautionary Statements:
P261-P305+P351+P338
Class:
-
Packing Group:
-

NMR Spectrum

Other Analytical Data

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Chemical Structure


Trichloropyridinegold(III) is a versatile compound widely utilized in chemical synthesis as a powerful catalyst. Its unique structure and properties make it highly effective in promoting various organic reactions, including C-C bond formation, functional group transformations, and asymmetric synthesis. With its exceptional catalytic activity and selectivity, Trichloropyridinegold(III) has become a valuable tool for chemists in the preparation of complex molecules with high efficiency and precision. Whether in academia or industry, this compound plays a crucial role in advancing the field of organic chemistry by enabling the development of new synthetic methodologies and the synthesis of important pharmaceuticals, agrochemicals, and materials.