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88963-39-7

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88963-39-7 Usage

General Description

2,3,6-Trichloroaniline is a chemical compound with the molecular formula C6H3Cl3N. It is an aromatic amine that is used as an intermediate in the production of dyes, pigments, and pharmaceuticals. 2,3,6-Trichloroaniline is a white to light tan solid that is insoluble in water but soluble in organic solvents. It is classified as a hazardous substance due to its potential to cause skin and eye irritation, and harmful effects if ingested or inhaled. Exposure to 2,3,6-Trichloroaniline should be minimized and proper safety precautions should be taken when handling this chemical.

Check Digit Verification of cas no

The CAS Registry Mumber 88963-39-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,8,9,6 and 3 respectively; the second part has 2 digits, 3 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 88963-39:
(7*8)+(6*8)+(5*9)+(4*6)+(3*3)+(2*3)+(1*9)=197
197 % 10 = 7
So 88963-39-7 is a valid CAS Registry Number.
InChI:InChI=1/C6H4Cl3N/c7-3-1-2-4(8)6(10)5(3)9/h1-2H,10H2

88963-39-7SDS

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 2,3,6-trichloroaniline

1.2 Other means of identification

Product number -
Other names 2,3,6-trichloro-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:88963-39-7 SDS

88963-39-7Relevant articles and documents

Novel Reactions: Part I - Facile Synthesis of Substituted ortho-Chloranilines from Nitrobenzene Derivatives

Ayyangar, N. R.,Kalkote, U. R.,Nikrad, P. V.

, p. 872 - 877 (2007/10/02)

N-Substituted benzo and acetohydroxamic acids (5), prepared from N-arylhydroxylamines and benzoyl or acetyl chloride, react readily with thionyl chloride at low temperature to give ortho-chloroanilide derivatives (6) in good yield.The latter (6) on hydrolysis give ortho-chloroanilines (10).Since the N-arylhydroxylamines are obtained from nitroarenes by partial reduction, the overall reaction amounts to the preparation of 10 from nitroarenes.

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