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Thiourea, N-2-benzothiazolyl-N-methyl- (9CI) is a chemical compound with the molecular formula C9H10N2S2. It is a derivative of thiourea, which is a sulfur-containing compound with the general formula (NH2)2CS. In this specific compound, the thiourea core is substituted with a benzothiazolyl group at the N position and a methyl group at the other N position. Benzothiazolyl is a heterocyclic aromatic ring system consisting of a benzene ring fused to a thiazole ring. Thiourea, N-2-benzothiazolyl-N-methyl- (9CI) is known for its potential applications in various chemical and pharmaceutical industries, such as in the synthesis of dyes, pigments, and pharmaceuticals. Due to its unique structure, it may exhibit specific properties and reactivity compared to other thiourea derivatives, making it a subject of interest for researchers in organic chemistry.

2741-05-1

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2741-05-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 2741-05-1 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, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 2741-05:
(6*2)+(5*7)+(4*4)+(3*1)+(2*0)+(1*5)=71
71 % 10 = 1
So 2741-05-1 is a valid CAS Registry Number.

2741-05-1SDS

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-(1,3-benzothiazol-2-yl)-3-methylthiourea

1.2 Other means of identification

Product number -
Other names Thiourea,N-2-benzothiazolyl-N'-methyl

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:2741-05-1 SDS

2741-05-1Relevant academic research and scientific papers

Dithiocarbamates, thiocarbamic esters, dithiocarboimidates, guanidines, thioureas, isothioureas, and tetraazathiapentalene derived from 2-aminobenzothiazole

Tellez, Fabiola,Cruz, Alejandro,Lopez-Sandoval, Horacio,Ramos-Garcia, Iris,Gayosso, Martha,Nely Castillo-Sierra,Paz-Michel, Brenda,Noeth, Heinrich,Flores-Parra, Angelina,Contreras, Rosalinda

, p. 4203 - 4214 (2007/10/03)

Reactions between CS2 and the exocyclic amino groups of 2-aminobenzothiazoles gave series of molecules bearing thiourea, isothiourea, dithiocarbamate, dithiocarboimine, dimethyldithiocarbamate, methyldithiocarbamate, S-CH3 and O-alkyl thiocarbarnic ester, and guanidine groups. Preferred tautomers and conformers were determined. Most compounds present coordinative bonds between the endocyclic sulfur atom, which behaves as a Lewis acid, and oxygen, nitrogen, and sulfur acting as bases. A new dibenzothiazolyltetraazathiapentalene containing a T-shaped hypervalent sulfur atom and displaying "single bond-no bond resonance" is discussed. X-ray structures of eleven compounds are reported. Wiley-VCH Verlag GmbH & Co. KGaA, 69451 Weinheim, Germany, 2004.

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