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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)-

Phosphonium, triphenyl(2-pyridinylmethyl)-, chloride, hydrochloride

c1ccc(nc1)C[P+](c1ccccc1)(c1ccccc1)c1ccccc1.Cl.[Cl-] Request for Quotation
Chemical Name: Phosphonium, triphenyl(2-pyridinylmethyl)-, chloride, hydrochloride
CAS Number: 99662-46-1
Product Number: AG003V5A(AGN-PC-00UNNB)
Synonyms:
MDL No:
Molecular Formula: C24H22Cl2NP
Molecular Weight: 426.317941

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Chemical Structure


Triphenyl(2-pyridylmethyl)phosphonium chloride hydrochloride is a versatile reagent widely used in chemical synthesis for its unique properties. It is particularly valuable in organic synthesis reactions such as the formation of carbon-carbon bonds, known as the Wittig reaction. This reagent plays a crucial role as a phosphonium ylide precursor, which allows for the efficient conversion of carbonyl compounds into alkenes, a key transformation in organic chemistry. Additionally, Triphenyl(2-pyridylmethyl)phosphonium chloride hydrochloride can be utilized in the synthesis of various heterocyclic compounds, pharmaceutical intermediates, and natural products due to its ability to introduce the phosphonium functionality into diverse molecular structures. This reagent offers chemists a powerful tool to access complex molecules through strategic bond forming reactions, making it an indispensable resource in the toolkit of synthetic chemists.