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Benzene, 1,3,5-trimethyl-2-[(4-nitrophenyl)thio]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

77189-94-7

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77189-94-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 77189-94-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,7,1,8 and 9 respectively; the second part has 2 digits, 9 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 77189-94:
(7*7)+(6*7)+(5*1)+(4*8)+(3*9)+(2*9)+(1*4)=177
177 % 10 = 7
So 77189-94-7 is a valid CAS Registry Number.

77189-94-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,5-trimethyl-2-(4-nitrophenyl)sulfanylbenzene

1.2 Other means of identification

Product number -
Other names 4-nitrophenyl 2',4',6'-trimethylphenyl sulfide

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:77189-94-7 SDS

77189-94-7Relevant academic research and scientific papers

Unsymmetrical Disulfides Synthesis via Sulfenium Ion

Parida, Amarchand,Choudhuri, Khokan,Mal, Prasenjit

supporting information, p. 2579 - 2583 (2019/07/15)

An umpolung approach for the synthesis of unsymmetrical disulfides via sulfenium ion is reported. In situ generated electrophilic sulfenium ion from electron-rich thiols reacted with second thiols to yield unsymmetrical disulfides. Using an iodine catalyst and 4-dimethylaminopyridine (DMAP)/water as promoter, the target syntheses were achieved in one pot under aerobic condition.

Iodine(III) Enabled Dehydrogenative Aryl C?S Coupling by in situ Generated Sulfenium Ion

Choudhuri, Khokan,Maiti, Saikat,Mal, Prasenjit

, p. 1092 - 1101 (2019/01/30)

Due to the normal polarity preferences, arenes form stable complexes with thiols through S?H???π interaction and direct dehydrogenative aryl C?S coupling is usually restricted. We report here an umpolung based one pot and direct C?S coupling approach unde

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