(5-Carboxypentyl)triphenylphosphonium bromide

• Catalog No.: 21935
• CAS Number: 50889-29-7
• M. F.: C24H26BrO2P
• M. W.: 457.339801
• Purity: ≥98.0%

SYNONYMS

• Title: (5-羧基戊基)三苯基溴化磷
• IUPAC name: (5-carboxypentyl)triphenylphosphanium bromide
• IUPAC Traditional name: (5-carboxypentyl)triphenylphosphanium bromide

DATABASE IDS

• CAS Number: 50889-29-7
• PubChem SID: 24853121
• MDL Number: MFCD00055556
• Beilstein Number: 4649483

PROPERTIES

• Linear Formula: (C6H5)3P(Br)(CH2)5COOH
• Purity: ≥98.0%
• Melting Point: 197-201 °C
• GHS Signal Word: Warning
• GHS Hazard statements: H315-H319-H335
• European Hazard Symbols: Irritant (Xi)
• Personal Protective Equipment: dust mask type N95 (US), Eyeshields, Gloves
• GHS Precautionary statements: P261-P305 + P351 + P338
• Risk Statements: 36/37/38
• Safety Statements: 26-36
• German water hazard class: 3

DETAILS

Description (English)

Application
Reactant for:
• Preparation of inhibitor of protein tyrosine phosphatase 1B for treatment of diabetes and obesity1
• Synthesis of folate receptor-specific glycinamide ribonucleotide formyltransferase inhibitors with antitumor activity2
• Preparation of peptide nucleic acids (PNA) with high specific activity3
• Synthesis of roseophilin via Wittig/aldol methodology4

Description (简体中文)

Application
Reactant for:
• Preparation of inhibitor of protein tyrosine phosphatase 1B for treatment of diabetes and obesity1
• Synthesis of folate receptor-specific glycinamide ribonucleotide formyltransferase inhibitors with antitumor activity2
• Preparation of peptide nucleic acids (PNA) with high specific activity3
• Synthesis of roseophilin via Wittig/aldol methodology4