Product

(4-Carboxybutyl)triphenylphosphonium bromide

CAS No.：17814-85-6

Other grades of this product :

(4-Carboxybutyl)triphenylphosphonium bromide Basic information

Product Name:	(4-Carboxybutyl)triphenylphosphonium bromide
Synonyms:	(4-CARBOXYBUTYL)TRIPHENYLPHOSPHONIUM BROMIDE;(4-Carboxybutyl)triphenylphosp;PhosphoniuM,(4-carboxybutyl)triphenyl-, broMide (1:1);4-carboxybutyltripheyl phosphonium bromide;(4-(4-carboxybutyl)phenyl)diphenylphosphonium bromide;4-carboxybutyl(triphenyl)phosphanium,bromide;(4-Carboxybut;(4-Carboxybut-1-yl)(triphenyl)phosphonium bromide 98%
CAS:	17814-85-6
MF:	C23H24BrO2P
MW:	443.31
EINECS:	241-782-5
Product Categories:	Miscellaneous Reagents;API intermediates;Miscellaneous Compounds;Phosphonium Compounds;Synthetic Organic Chemistry;Wittig & Horner-Emmons Reaction;Wittig Reaction;C-C Bond Formation;Olefination;Wittig Reagents
Mol File:	17814-85-6.mol

(4-Carboxybutyl)triphenylphosphonium bromide Chemical Properties

Melting point	204-207 °C(lit.)
Boiling point	324.7-327.4℃ at 101.93-102.15kPa
density	1.371 at 20℃
vapor pressure	0Pa at 25℃
Fp	195°(383°F)
storage temp.	Store below +30°C.
solubility	DMSO, Methanol, Water
form	solid
color	White to Off-White
Water Solubility	Soluble in ethanol, methanol and soluble water. Insoluble in toluene and hexane.
Sensitive	Hygroscopic
BRN	3586477
InChIKey	KQJPHSBFOSLICV-UHFFFAOYSA-N
LogP	0.146
CAS DataBase Reference	17814-85-6(CAS DataBase Reference)

Safety Information

Hazard Codes	Xi
Risk Statements	36/37/38
Safety Statements	26-36
RIDADR	3278
WGK Germany	3
HS Code	29310095

MSDS Information

Provider	Language
(4-Carboxybutyl)triphenylphosphonium bromide	English
SigmaAldrich	English
ALFA	English

(4-Carboxybutyl)triphenylphosphonium bromide Usage And Synthesis

Chemical Properties	WHITE TO ALMOST WHITE CRYSTALLINE POWDER
Uses	suzuki reaction
Uses	(4-Carboxybutyl)triphenylphosphonium Bromide (cas# 17814-85-6) is a compound useful in organic synthesis.
Uses	Used as a platform for delivery of pro-apoptotic peptides into the mitochondria of tumor cells Reactant for preparation of: Ring skeletons via ring closing metathesis and double bond migration ring closing metathesis reactions Methyl alkenyl quinolones as antimycobacterial agents Prostaglandins and their drug analogs via Gold-catalyzed Meyer-Schuster rearrangement Diphenylmethylpiperazines as N-type calcium channel blockers as potential therapeutic agents Folate receptor-specific glycinamide ribonucleotide formyltransferase (GARFTase) inhibitors with antitumor activity Cycloalkylidene alkanols with antileishmanial activity, via Wittig reaction

(4-Carboxybutyl)triphenylphosphonium bromide Preparation Products And Raw materials

Preparation Products

6-PHENYL-1-HEXANOL-->Travoprost Acid-->(+)-Cloprostenol

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