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101703-31-5

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101703-31-5 Usage

General Description

2-Bromo-4,6-dimethylaniline hydrogen bromide is a chemical compound that contains a bromide ion and a dimethylamino group. It is commonly used in organic synthesis and pharmaceuticals as a reagent for the preparation of various derivatives. 2-BroMo-4,6-diMethylaniline hydrogen broMide is also known for its antifungal properties and is used in the production of veterinary and human medicines. It is important to handle this compound with care due to its potential hazards, including skin and eye irritation, and it should only be used by trained professionals in a controlled laboratory environment.

Check Digit Verification of cas no

The CAS Registry Mumber 101703-31-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,0,1,7,0 and 3 respectively; the second part has 2 digits, 3 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 101703-31:
(8*1)+(7*0)+(6*1)+(5*7)+(4*0)+(3*3)+(2*3)+(1*1)=65
65 % 10 = 5
So 101703-31-5 is a valid CAS Registry Number.

101703-31-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name 2-Bromo-4,6-dimethylaniline hydrobromide (1:1)

1.2 Other means of identification

Product number -
Other names 2-bromo-4,6-dimethylaniline hydrobromide

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:101703-31-5 SDS

101703-31-5Upstream product

101703-31-5Relevant articles and documents

Process for the preparation of biphenyl intermediates

-

, (2008/06/13)

A novel process for the preparation of intermediates in the totally synthetic antihypercholesterolemic agents, 6-[2-[1,1'-biphenyl]-2-yl-ethenyl] pyranones, involving a highly efficient nickel catalyzed aryl cross-coupling reaction is disclosed.

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