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22235-32-1

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22235-32-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 22235-32-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,2,3 and 5 respectively; the second part has 2 digits, 3 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 22235-32:
(7*2)+(6*2)+(5*2)+(4*3)+(3*5)+(2*3)+(1*2)=71
71 % 10 = 1
So 22235-32-1 is a valid CAS Registry Number.

22235-32-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name [difluoro(phenyl)methyl]sulfanylbenzene

1.2 Other means of identification

Product number -
Other names -

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:22235-32-1 SDS

22235-32-1Relevant articles and documents

DIFLUOROMETHYL AND DIFLUOROMETHYLENE TRANSFER REAGENTS

-

Paragraph 0094, (2020/01/22)

Disclosed herein are borazine, borate, and azaborinine compounds and compositions, methods of making said compounds and compositions, and methods of forming aromatic difluorocarbon compounds and difluorocarbon compounds.

Reactions of (chlorodifluoromethyl)benzene and (chlorodifluoromethoxy) benzene with nucleophilic reagents

Guidotti, Jér?me,Schanen, Vincent,Tordeux, Marc,Wakselman, Claude

, p. 445 - 449 (2007/10/03)

Condensation reactions of (chlorodifluoromethyl)benzene and (chlorodifluoromethoxy)benzene with phenoxide and thiophenoxide ions have been performed in DMF or NMP with heating. In these conditions, the reaction between phenylselenide ion and (chlorodifluo

Anodic gem-Difluorination of Dithioacetals

Yoshiyama, Tomonori,Fuchigami, Toshio

, p. 1995 - 1998 (2007/10/02)

Anodic desulfurization of dithioacetals of ketones in the presence of Et3N*3HF provided the corresponding gem-difluorocompounds while dithioacetals of aromatic and aliphatic aldehydes gave gem-difluorothioethers and monofluoro thioether, respectively.

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