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3,3'-Dimethyl-4,4'-sulfinyl-di-phenol is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

14763-66-7

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14763-66-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 14763-66-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,4,7,6 and 3 respectively; the second part has 2 digits, 6 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 14763-66:
(7*1)+(6*4)+(5*7)+(4*6)+(3*3)+(2*6)+(1*6)=117
117 % 10 = 7
So 14763-66-7 is a valid CAS Registry Number.

14763-66-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,3'-Dimethyl-4,4'-sulfinyl-di-phenol

1.2 Other means of identification

Product number -
Other names Bis-(4-hydroxy-2-methyl-phenyl)-sulfoxid

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:14763-66-7 SDS

14763-66-7Relevant academic research and scientific papers

Selective synthesis of sulfoxides and sulfones from sulfides using silica bromide as the heterogeneous promoter and hydrogen peroxide as the terminal oxidant

Maleki, Behrooz,Hemmati, Saba,Sedrpoushan, Alireza,Ashrafi, Samaneh Sedigh,Veisi, Hojat

, p. 40505 - 40510 (2015/02/03)

Silica bromide as a heterogeneous promoter and reagent is prepared from the reaction of silica gel with PBr3as a non-hydroscopic, filterable, cheap, and stable yellowish powder that can be stored for months. The results show that silica bromide is a suitable and efficient promoter for the chemoselective oxidation of sulfides to the corresponding sulfoxides or sulfones in the presence of 30% H2O2in acetonitrile. The excellent yields, heterogeneous conditions, simplicity, compatibility with a variety of functionalities, and ease of isolation of the products make our procedure a practical alternative.

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