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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, [[4-(methoxycarbonyl)phenyl]methyl]triphenyl-, chloride

COC(=O)c1ccc(cc1)C[P+](c1ccccc1)(c1ccccc1)c1ccccc1.[Cl-] Request for Quotation
Chemical Name: Phosphonium, [[4-(methoxycarbonyl)phenyl]methyl]triphenyl-, chloride
CAS Number: 1253-47-0
Product Number: AG000NGG(AGN-PC-01NPX1)
Synonyms:
MDL No:
Molecular Formula: C27H24ClO2P
Molecular Weight: 446.9050

Identification/Properties

Properties
MP:
258-260℃
Form:
Solid

Safety Information

NMR Spectrum

Other Analytical Data

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Chemical Structure


The compound (4-(Methoxycarbonyl)benzyl)triphenylphosphonium chloride plays a crucial role in chemical synthesis as a versatile and efficient reagent. This compound is commonly used in organic chemistry reactions, particularly in the field of phosphonium salt chemistry. Its unique structure allows for a wide range of applications in various synthetic methodologies.In chemical synthesis, (4-(Methoxycarbonyl)benzyl)triphenylphosphonium chloride can act as a strong carbon nucleophile due to the presence of the triphenylphosphonium group. This reactivity makes it an excellent choice for reactions involving carbon-carbon bond formation, such as the Wittig reaction and Michael addition reactions. Additionally, the methoxycarbonyl benzyl group can be easily deprotected under mild conditions, allowing for further functional group manipulations in the synthesis of complex organic compounds.Furthermore, the phosphonium chloride moiety in this compound provides stability and facilitates its use in various reaction conditions. Its compatibility with a wide range of solvents and reaction conditions makes it a valuable tool for organic chemists looking to streamline their synthetic strategies and achieve high yields of desired products. The ability of (4-(Methoxycarbonyl)benzyl)triphenylphosphonium chloride to participate in diverse chemical transformations highlights its importance in modern organic synthesis methodologies.