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7466-04-8

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7466-04-8 Usage

Molecular structure

Consists of a trichlorophenyl group (a benzene ring with three chlorine atoms) and a 4-methylbenzenesulfonate group (a benzene ring with a methyl group and a sulfonate group).

Usage

Mainly used as an intermediate in the production of pharmaceuticals, agrochemicals, and dyes. Also used as a solvent in organic synthesis.

Antimicrobial properties

Studied for its potential as a disinfectant and fungicide.

Safety precautions

Can be harmful if swallowed, inhaled, or comes in contact with the skin or eyes. It is important to handle this chemical with care and follow safety protocols.

Check Digit Verification of cas no

The CAS Registry Mumber 7466-04-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,6 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7466-04:
(6*7)+(5*4)+(4*6)+(3*6)+(2*0)+(1*4)=108
108 % 10 = 8
So 7466-04-8 is a valid CAS Registry Number.
InChI:InChI=1/C13H9Cl3O3S/c1-8-2-4-10(5-3-8)20(17,18)19-13-11(15)6-9(14)7-12(13)16/h2-7H,1H3

7466-04-8SDS

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-trichlorophenyl) 4-methylbenzenesulfonate

1.2 Other means of identification

Product number -
Other names 2,4,6-trichlorophenyltosylate

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:7466-04-8 SDS

7466-04-8Relevant articles and documents

Trichlorophenol (TCP) sulfonate esters: A selective alternative to pentafluorophenol (PFP) esters and sulfonyl chlorides for the preparation of sulfonamides

Wilden, Jonathan D.,Geldeard, Lynsey,Lee, Chieh C.,Judd, Duncan B.,Caddick, Stephen

, p. 1074 - 1076 (2007/12/29)

2,4,6-Trichlorophenol (TCP) sulfonate esters undergo effective aminolysis under conventional heating and microwave irradiation; the reactivity of these species is such that chemoselective transformations of PFP sulfonate esters can be achieved. The Royal Society of Chemistry.

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