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(4-Methylphenyl)-triphenylphosphonium bromide is a quaternary phosphonium salt with the chemical formula C19H17BrP. It is a white to off-white crystalline solid that is insoluble in water but soluble in organic solvents such as ethanol and acetone.

6031-78-3

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6031-78-3 Usage

Uses

Used in Organic Synthesis:
(4-Methylphenyl)-triphenylphosphonium bromide is used as a phase-transfer catalyst for facilitating the transfer of reactants or reagents from one phase to another in organic synthesis reactions.
Used in Catalysis:
(4-Methylphenyl)-triphenylphosphonium bromide is used as a catalyst in a variety of reactions, including the Wittig reaction and the Grignard reaction.
Used in Antimicrobial and Antifungal Applications:
(4-Methylphenyl)-triphenylphosphonium bromide has been studied for its potential antimicrobial and antifungal properties, making it a versatile and useful compound in various scientific research and industrial applications.

Check Digit Verification of cas no

The CAS Registry Mumber 6031-78-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,3 and 1 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6031-78:
(6*6)+(5*0)+(4*3)+(3*1)+(2*7)+(1*8)=73
73 % 10 = 3
So 6031-78-3 is a valid CAS Registry Number.

6031-78-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name (4-methylphenyl)-triphenylphosphanium,bromide

1.2 Other means of identification

Product number -
Other names Triphenyl-p-tolyl-phosphoniumbromid

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6031-78-3 SDS

6031-78-3Downstream Products

6031-78-3Relevant academic research and scientific papers

Ionic liquids of superior thermal stability

Cassity, Cody G.,Mirjafari, Arsalan,Mobarrez, Niloufar,Strickland, Katie J.,O'Brien, Richard A.,Davis, James H.

, p. 7590 - 7592 (2013/08/28)

In a head-to-head study, ILs based upon tetraarylphosphonium cations exhibit superior long-term thermal stability compared to familiar salts based upon imidazolium, quaternary ammonium, or tetraalkylphosphonium cations. The Royal Society of Chemistry.

Palladium-catalyzed synthesis of functionalized tetraarylphosphonium salts

Marcoux, David,Charette, Andre B.

, p. 590 - 593 (2008/09/17)

(Chemical Equation Presented) An efficient method to synthesize functionalized tetraarylphosphonium salts is described. This palladium-catalyzed coupling reaction between aryl iodides, bromides, or triflates and triphenylphosphine generates phosphonium salts in high yields. The coupling is compatible with a variety of functional groups such as alcohols, ketones, aldehydes, phenols, and amides.

Convenient Preparation of Tetraarylphosphonium Halides

Migita, Toshihiko,Nagai, Tohru,Kiuchi, Kazuhiko,Kosugi, Masanori

, p. 2869 - 2870 (2007/10/02)

Tetraarylphosphonium halides, particularly iodides, can be conveniently prepared by the Pd-catalyzed reaction of aryl halides and triarylphosphines in good yields.

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