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5400-76-0

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5400-76-0 Usage

General Description

2,4,6-trichloro-3-methyl-aniline is a chemical compound with a molecular formula C7H6Cl3N. It is a derivative of aniline, with three of its hydrogen atoms replaced by chlorine atoms and one of its methyl groups. 2,4,6-trichloro-3-methyl-aniline is used in the synthesis of various pharmaceuticals and pesticides. It is a pale yellow to brown solid with a slight amine odor. It is classified as a hazardous substance and should be handled with care due to its toxic and potentially carcinogenic properties.

Check Digit Verification of cas no

The CAS Registry Mumber 5400-76-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,4,0 and 0 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 5400-76:
(6*5)+(5*4)+(4*0)+(3*0)+(2*7)+(1*6)=70
70 % 10 = 0
So 5400-76-0 is a valid CAS Registry Number.
InChI:InChI=1/C7H6Cl3N/c1-3-4(8)2-5(9)7(11)6(3)10/h2H,11H2,1H3

5400-76-0SDS

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 2,4,6-trichloro-3-methylaniline

1.2 Other means of identification

Product number -
Other names 2,4,6-trichloro-3-methyl-aniline

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:5400-76-0 SDS

5400-76-0Relevant articles and documents

Synthesis of 2,6-disubstituted and 2,3,6-trisubstituted anilines

Pews,Hunter,Wehrmeyer

, p. 4809 - 4820 (2007/10/02)

A number of 2,6-disubstituted and 2,3,6-trisubstituted anilines have been prepared via the selective para dehalogenation of the corresponding anilines. Modification of the substituents on the amino nitrogen demonstrates that the selectivity is derived from steric rather than electronic effects. The effects of the choice of formate hydrogen donor, Pd catalyst, solvent, and temperature upon the efficiency and selectivity of the dehalogenation are discussed.

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