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6358-15-2

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6358-15-2 Usage

General Description

Solid.

Air & Water Reactions

May be sensitive to prolonged exposure to air.

Reactivity Profile

2-amino-3,4,6-trichlorophenol may react with strong oxidizing agents and mineral acids or bases .

Fire Hazard

Flash point data for 2-amino-3,4,6-trichlorophenol are not available. 2-amino-3,4,6-trichlorophenol is probably combustible.

Check Digit Verification of cas no

The CAS Registry Mumber 6358-15-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,5 and 8 respectively; the second part has 2 digits, 1 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 6358-15:
(6*6)+(5*3)+(4*5)+(3*8)+(2*1)+(1*5)=102
102 % 10 = 2
So 6358-15-2 is a valid CAS Registry Number.
InChI:InChI=1/C6H4Cl3NO/c7-2-1-3(8)6(11)5(10)4(2)9/h1,11H,10H2

6358-15-2SDS

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 2-amino-3,4,6-trichlorophenol

1.2 Other means of identification

Product number -
Other names 3,4,6-Trichlor-2-aminophenol

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:6358-15-2 SDS

6358-15-2Upstream product

6358-15-2Relevant articles and documents

A new intramolecular migration of the imino group of O-arylketoximes to the aryl group under the Beckmann condition

Kikugawa, Yasuo,Tsuji, Chiho,Miyazawa, Etsuko,Sakamoto, Takeshi

, p. 2337 - 2339 (2007/10/03)

ZrCl4-mediated decomposition of O-arylketoximes in benzene leads to regioselective intramolecular migration of the imino group from the oxygen to the ortho position of the aryl group via electron-deficient nitrogen intermediates.

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