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1,1-dimethyl-3-m-tolylthiourea is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

21540-35-2

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21540-35-2 Usage

Uses

1,1-Dimethyl-3-(meta-tolyl)-2-thiourea is used in herbicidal/pesticidal/ formulations.

Check Digit Verification of cas no

The CAS Registry Mumber 21540-35-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,5,4 and 0 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 21540-35:
(7*2)+(6*1)+(5*5)+(4*4)+(3*0)+(2*3)+(1*5)=72
72 % 10 = 2
So 21540-35-2 is a valid CAS Registry Number.
InChI:InChI=1/C10H14N2S/c1-8-5-4-6-9(7-8)11-10(13)12(2)3/h4-7H,1-3H3,(H,11,13)

21540-35-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name methiuron

1.2 Other means of identification

Product number -
Other names 1,1-dimethyl-3-(3-methylphenyl)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:21540-35-2 SDS

21540-35-2Relevant academic research and scientific papers

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.

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