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2589-31-3

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2589-31-3 Usage

Type of compound

Quaternary ammonium salt

Structure

Benzyl group attached to the nitrogen atom of a pyridinium cation

Common uses

a. Phase-transfer catalyst in organic synthesis
b. Antimicrobial agent
c. Potential applications in drug delivery systems
d. Intermediate in the synthesis of pharmaceuticals and other organic compounds

Physical appearance

White solid

Solubility

Low solubility in water

Handling and storage

Typically handled and stored under inert gas and away from moisture and oxidizing agents

Check Digit Verification of cas no

The CAS Registry Mumber 2589-31-3 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,5,8 and 9 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 2589-31:
(6*2)+(5*5)+(4*8)+(3*9)+(2*3)+(1*1)=103
103 % 10 = 3
So 2589-31-3 is a valid CAS Registry Number.

2589-31-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-benzylpyridinium bromide

1.2 Other means of identification

Product number -
Other names benzylpyridinium bromide

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:2589-31-3 SDS

2589-31-3Relevant articles and documents

Rational selection of the cation of an ionic liquid to control the reaction outcome of a substitution reaction

Hawker, Rebecca R.,Haines, Ronald S.,Harper, Jason B.

, p. 2296 - 2299 (2018)

A range of ionic liquids was examined as solvents for a substitution reaction. They were chosen through rationally varying the ionic liquid cation in order to enhance the rate constant. Access to charge and electron-withdrawing substituents benefitted rat

Understanding the effects of solvate ionic liquids as solvents on substitution processes

Schaffarczyk McHale, Karin S.,Wong, Michaela J.,Evans, Alicia K.,Gilbert, Alyssa,Haines, Ronald S.,Harper, Jason B.

, p. 9243 - 9250 (2019)

The effects of solvate ionic liquids as solvents have been considered for two substitution processes where the solvent effects of typical ionic liquids have been extensively investigated previously; the bimolecular nucleophilic substitution (SN

Novel antimonate luminescent material Luminescent film and preparation method thereof

-

Paragraph 0031-0033, (2021/06/21)

The invention belongs to the technical field of functional materials, in particular to a novel antimonate bromide luminescent material. The benzyl substituted pyridinium pentabromide antimonate is a compound composed of antimony pentabromide anions and be

Are pyridinium ylides radicals?

Liao, Fan,Huang, Wenhuan,Chen, Biao,Ding, Zijing,Li, Xingxing,Su, Hao,Wang, Tao,Wang, Yucai,Miao, Hui,Zhang, Xiaolong,Luo, Yi,Yang, Jinlong,Zhang, Guoqing

supporting information, p. 11287 - 11290 (2020/10/06)

Pyridinium ylides are usually considered nucleophiles that can undergo various reactions involving electron pairs. However, it was found that ylides resulting from deprotonation ofN-alkyl-substituted pyridinium salts exhibit radical characters, with no di

ENANTIOMERIC COMPOUNDS

-

Page/Page column 24, (2020/05/07)

The present invention relates to enantiomeric compounds, their use in stereospecific reactions and to a method of preparing enantiomeric compounds.

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