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2741-12-0

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2741-12-0 Usage

General Description

1,1-dimethyl-3-(2-methylphenyl)thiourea is a chemical compound with the molecular formula C11H16N2S. It is a thiourea derivative with a dimethyl-substituted terminal nitrogen and a 2-methylphenyl group. 1,1-dimethyl-3-(2-methylphenyl)thiourea is commonly used as a catalyst or as an intermediate in the production of dyes, pharmaceuticals, and other organic compounds. It is also known for its potential biological activities, such as anti-inflammatory and antioxidant properties. However, it is important to handle this chemical with care as it may pose health risks if not properly managed and disposed of.

Check Digit Verification of cas no

The CAS Registry Mumber 2741-12-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 2,7,4 and 1 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 2741-12:
(6*2)+(5*7)+(4*4)+(3*1)+(2*1)+(1*2)=70
70 % 10 = 0
So 2741-12-0 is a valid CAS Registry Number.

2741-12-0SDS

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 1,1-dimethyl-3-(2-methylphenyl)thiourea

1.2 Other means of identification

Product number -
Other names N,N-dimethyl-N'-o-tolyl-thiourea

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:2741-12-0 SDS

2741-12-0Relevant articles and documents

Use of tetramethylthiuram disulfide in synthesis of nitrogen-containing heterocyclic compounds

Demchenko,Yanchenko,Kisly,Lozinskii

, p. 668 - 672 (2007/10/03)

We have developed a method for synthesis of aryl isothiocyanates by means of thiocarbamoylation of aromatic amines by tetramethylthiuram disulfide followed by degradation of the intermediate N(1)-aryl-N,N- dimethylthiourea by concentrated HCl. We have shown that thiocarbamoylation of 4-amino-5-ethyl-4H-1,2,4-triazole-3-thiol occurs at the 2 position of the triazole ring, while thiocarbamoylation of 4-amino-3-methyl-6-phenyl-4,5- dihydro-1,2,4-triazin-5-one leads to the dihetaryl-substituted thiourea. We consider the possibility of using N(1)-aryl-N,N-dimethylthioureas as analogs of isothiocyanates in reactions with N-nucleophiles. 2005 Springer Science+Business Media, Inc.

A convenient route to substituted thiocarbamides

Ramadas,Srinivasan

, p. 3381 - 3387 (2007/10/03)

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