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67013-54-1

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67013-54-1 Usage

Molecular Weight

264.43 g/mol

Structure

A benzene ring with a chlorine atom in the first position and a dibromomethyl group in the second position.

Group

Benzene derivatives

Usage

主要用于chemical reactions and synthesis processes, primarily as an intermediate in the production of pharmaceuticals, agrochemicals, and other organic compounds.

Value

Unique chemical structure makes it valuable for the modification and synthesis of other organic molecules.

Hazards

需注意, as it is considered hazardous and can cause harm to human health and the environment if not properly managed.

Check Digit Verification of cas no

The CAS Registry Mumber 67013-54-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,7,0,1 and 3 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 67013-54:
(7*6)+(6*7)+(5*0)+(4*1)+(3*3)+(2*5)+(1*4)=111
111 % 10 = 1
So 67013-54-1 is a valid CAS Registry Number.
InChI:InChI=1/C7H5Br2Cl/c8-7(9)5-3-1-2-4-6(5)10/h1-4,7H

67013-54-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1-chloro-2-(dibromomethyl)benzene

1.2 Other means of identification

Product number -
Other names o-chlorobenzal 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:67013-54-1 SDS

67013-54-1Relevant articles and documents

A simple and efficient procedure for the preparation of benzal chlorides and benzal bromides

Léonel, Eric,Paugam, Jean-Paul,Heintz, Monique,Nédélec, Jean-Yves

, p. 4015 - 4024 (2007/10/03)

Benzal chlorides and benzal bromides were conveniently synthesized by reaction of aryl aldehydes with a Vilsmeier type reagent formed in situ by reduction of CCl4 or CBr4 in dimethylformamide (DMF) as solvent.

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