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51431-75-5

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51431-75-5 Usage

General Description

1,3,5-trimethyl-2-{[4-(trifluoromethyl)phenyl]sulfanyl}benzene is a chemical compound with a molecular formula C17H16F3S. It is a benzene derivative with three methyl groups on the 1st, 3rd, and 5th positions and a trifluoromethyl group attached to a phenyl ring that is thiolated. 1,3,5-trimethyl-2-{[4-(trifluoromethyl)phenyl]sulfanyl}benzene is widely utilized in various fields, including pharmaceuticals, agrochemicals, and materials science. It has been studied for its potential use in organic light-emitting diodes, as well as its antimicrobial and anti-inflammatory properties. Additionally, this chemical structure is used as a building block in the synthesis of other specialized organic compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 51431-75-5 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,4,3 and 1 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51431-75:
(7*5)+(6*1)+(5*4)+(4*3)+(3*1)+(2*7)+(1*5)=95
95 % 10 = 5
So 51431-75-5 is a valid CAS Registry Number.

51431-75-5SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 14, 2017

Revision Date: Aug 14, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,5-trimethyl-2-[4-(trifluoromethyl)phenyl]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:51431-75-5 SDS

51431-75-5Relevant articles and documents

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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