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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)-

Phosphinous chloride, bis[3,5-bis(1,1-dimethylethyl)-4-methoxyphenyl]-

COc1c(cc(cc1C(C)(C)C)P(c1cc(c(c(c1)C(C)(C)C)OC)C(C)(C)C)Cl)C(C)(C)C Request for Quotation
Chemical Name: Phosphinous chloride, bis[3,5-bis(1,1-dimethylethyl)-4-methoxyphenyl]-
CAS Number: 212713-08-1
Product Number: AG003O95(AGN-PC-09T517)
Synonyms:
MDL No:
Molecular Formula: C30H46ClO2P
Molecular Weight: 505.111801

Identification/Properties

Properties
Storage:
2-8℃;Light sensitive;Inert atmosphere;

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


Bis(3,5-di-tert-butyl-4-methoxyphenyl)chlorophosphine is a versatile chemical reagent commonly used in chemical synthesis. It serves as a powerful ligand in coordination chemistry, forming stable complexes with various metal ions. This compound is particularly valuable in catalytic reactions due to its ability to promote selective bond formation and facilitate complex transformations.In organic synthesis, Bis(3,5-di-tert-butyl-4-methoxyphenyl)chlorophosphine plays a crucial role as a catalyst or co-catalyst in a wide range of reactions. Its presence can enhance reaction rates, improve yields, and influence the stereochemistry of the products. This compound is especially useful in asymmetric synthesis, where the control of chirality is essential in obtaining desired enantiomeric excesses.Furthermore, Bis(3,5-di-tert-butyl-4-methoxyphenyl)chlorophosphine is employed in cross-coupling reactions, hydrogenation processes, and C-H activation methodologies. Its unique structural features and reactivity make it an indispensable tool in the toolkit of synthetic chemists aiming to access complex molecules efficiently and selectively.