(5-Carboxypentyl)(triphenyl)phosphonium bromide 50889-29-7

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(5-Carboxypentyl)(triphenyl)phosphonium bromide 50889-29-7

(5-Carboxypentyl)(triphenyl)phosphonium bromide CAS 50889-29-7

Name:    (5-Carboxypentyl)(triphenyl)phosphonium bromide
Synonyms:    (5-CARBOXYPENTYL)TRIPHENYLPHOSPHONIUM BROMIDE;(5-CARBOXYAMYL)TRIPHENYLPHOSPHONIUM BROMIDE;(5-Carboxypentyl)(triphenyl)phosphonium bromide 97%;5-carboxypentyltriphenylphosphonium bromide, 98 %;(5-Carboxypentyl)triphenylphosphoniumbromide,97%
CAS:    50889-29-7
MF:    C24H26BrO2P
MW:    457.34
EINECS:    
Product Categories:    All Aliphatics;Miscellaneous Compounds;Aliphatics;Wittig Reagents
Mol File:    50889-29-7.mol
(5-Carboxypentyl)(triphenyl)phosphonium bromide Structure
(5-Carboxypentyl)(triphenyl)phosphonium bromide Chemical Properties
Melting point     197-201 °C
solubility     Soluble in Chloroform and Methanol.
Sensitive     Hygroscopic
CAS DataBase Reference    50889-29-7(CAS DataBase Reference)
Safety Information
Hazard Codes     Xi,Xn
Risk Statements     36/37/38-20/21/22
Safety Statements     26-36-36/37/39-22
WGK Germany     3
MSDS Information

Properties
Appearance & Physical State     white crystalline solid
Melting Point     200-202ºC
Safety Info
Safety Statements     S22-S26-S36/37/39

(5-Carboxypentyl)(triphenyl)phosphonium bromide Usage And Synthesis
Chemical Properties    White Crystalline Solid
Uses    (5-Carboxypentyl)(triphenyl)phosphonium bromide is used in medicine and as pharmaceutical intermediate. It is also employed as catalyst.
Reactant for:

    Preparation of inhibitor of protein tyrosine phosphatase 1B for treatment of diabetes and obesity.
    Synthesis of folate receptor-specific glycinamide ribonucleotide formyltransferase inhibitors with antitumor activity.
    Preparation of peptide nucleic acids (PNA) with high specific activity.
    Synthesis of roseophilin via Wittig/aldol methodology.

(5-Carboxypentyl)(triphenyl)phosphonium bromide Preparation Products And Raw materials