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651-84-3

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651-84-3 Usage

Chemical Properties

clear colorless liquid

Check Digit Verification of cas no

The CAS Registry Mumber 651-84-3 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 6,5 and 1 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 651-84:
(5*6)+(4*5)+(3*1)+(2*8)+(1*4)=73
73 % 10 = 3
So 651-84-3 is a valid CAS Registry Number.
InChI:InChI=1/C7HF7S/c8-2-1(7(12,13)14)3(9)5(11)6(15)4(2)10/h15H

651-84-3SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3,5,6-tetrafluoro-4-(trifluoromethyl)benzenethiol

1.2 Other means of identification

Product number -
Other names PC7769C

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:651-84-3 SDS

651-84-3Relevant articles and documents

Reactions of polyfluorobenzenethiols with polyhalomethanes and their derivatives in an alkaline medium

Bredikhin,Maksimov,Gatilov, Yu. V.,Kireenkov,Platonov

, p. 1551 - 1559 (2015/12/30)

New process direction was found in the reaction of polyfluoroarenethiols with fluorodichloromethane, chloroform, and bromoform in an alkaline medium consisting in the replacement of the thiol group by a hydrogen atom. This process competes with the formation of expected products, dihalomethyl polyfluoro-aryl sulfides and tris(arylsulfanyl)methanes. In reaction of 2,3,5,6-tetrafluorobenzenethiol with dichloro-methane bis(2,3,5,6-tetrafluorophenylsulfanyl)methane was obtained. Reactions of polyfluoroarenethiols with pentafluorobenzyl chloride occur mainly with the substitution of the chlorine atom, with pentafluorobenzal chloride and with pentafluorobenzotrichloride a substitution of a fluorine atom in the para-position takes place.

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