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2(3H)-Benzothiazolone, 5-methyl-(9CI), also known as 5-Methylbenzothiazolone, is an organic compound belonging to the benzothiazolone family. It features a benzene ring fused to a thiazole ring and has the molecular formula C9H7NOS. This yellow crystalline solid is sparingly soluble in water but more soluble in organic solvents. As a building block in the chemical industry, it is used in the synthesis of pharmaceuticals and agrochemicals.

40925-61-9

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40925-61-9 Usage

Uses

Used in Pharmaceutical Industry:
2(3H)-Benzothiazolone, 5-methyl-(9CI) is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique chemical structure allows it to be incorporated into drug molecules, potentially enhancing their therapeutic properties and effectiveness.
Used in Agrochemical Industry:
In the agrochemical industry, 2(3H)-Benzothiazolone, 5-methyl-(9CI) serves as a crucial building block for the development of new agrochemicals. Its incorporation into these compounds can lead to improved pest control and crop protection.
Used in Chemical Synthesis:
2(3H)-Benzothiazolone, 5-methyl-(9CI) is utilized as a versatile building block in the synthesis of various organic compounds. Its unique structure and reactivity make it a valuable component in the creation of new chemical entities with potential applications in various industries.

Check Digit Verification of cas no

The CAS Registry Mumber 40925-61-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 4,0,9,2 and 5 respectively; the second part has 2 digits, 6 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 40925-61:
(7*4)+(6*0)+(5*9)+(4*2)+(3*5)+(2*6)+(1*1)=109
109 % 10 = 9
So 40925-61-9 is a valid CAS Registry Number.

40925-61-9SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 5-Methylbenzo[d]thiazol-2(3H)-one

1.2 Other means of identification

Product number -
Other names 5-methyl-3H-1,3-benzothiazol-2-one

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:40925-61-9 SDS

40925-61-9Downstream Products

40925-61-9Relevant academic research and scientific papers

Synthesis of benzimidazolones, benzooxazolones, 2-amino-benzothiazoles from ethyl cyanoformate and o-phenylene Diamines, o-aminophenols, oaminothiophenols Promoted by Lithium Bromide ;

Dekhane, Deepak V.,Pawara, Shivaji V.,Gupta, Sunil V.,Shingareb, Murlidhar S.,Thore, Shivaji N.

experimental part, p. 406 - 411 (2012/05/04)

The lithium bromide mediated condensation of 1-amino-2-heteroaryl substrates with ethyl cyanoformate, to obtain versatile alkylcarbamate protected benzoheteroazolones was studied. This unprecedented reaction could be used to furnish different azolones like 2-benzimidazolones, 2-benooxazolones and 2-amino-thiazoles in good yields. 2011 Bentham Science Publishers Ltd.

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