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710967-01-4

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710967-01-4 Usage

Structure

Contains a sulfur atom, a benzene ring, and an aniline group

Classification

Sulfanyl aniline derivative

Usage

Building block for the preparation of biologically active molecules and pharmaceuticals, reagent in the synthesis of heterocyclic compounds, precursor for the preparation of dyes and pigments

Hazard

Potentially hazardous chemical, requires proper care and safety precautions

Check Digit Verification of cas no

The CAS Registry Mumber 710967-01-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 7,1,0,9,6 and 7 respectively; the second part has 2 digits, 0 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 710967-01:
(8*7)+(7*1)+(6*0)+(5*9)+(4*6)+(3*7)+(2*0)+(1*1)=154
154 % 10 = 4
So 710967-01-4 is a valid CAS Registry Number.

710967-01-4SDS

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 2-[(3-methylphenyl)methylsulfanyl]aniline

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:710967-01-4 SDS

710967-01-4Downstream Products

710967-01-4Relevant articles and documents

Di- tert-butyl Peroxide-Mediated Radical C(sp2/sp3)-S Bond Cleavage and Group-Transfer Cyclization

Luo, Kai,Yang, Wen-Chao,Wei, Kai,Liu, Yue,Wang, Jun-Ke,Wu, Lei

supporting information, p. 7851 - 7856 (2019/10/11)

A novel strategy of cascade radical C(sp2/sp3)-S bond cleavage and group-transfer cyclization is disclosed. Triggered by alkyl radicals, varieties of 2-isocyanoaryl thioethers containing aliphatic, aryl, and heteroaromatic groups can be cleaved and precisely reinstalled to give benzothiazole derivatives. Mechanistic studies reveal that the cascade reaction undertakes an intermolecular pathway, and the inner radical sources (R radicals) exhibit high priority over those of methyl radical origin from di-tert-butyl peroxide.

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