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3,5-bis(methylsulfonyl)-1,2-thiazole-4-carbonitrile is a complex organic chemical compound with the molecular formula C6H6N2O4S3. It features a 1,2-thiazole ring, which is a five-membered heterocyclic ring containing sulfur and nitrogen atoms. The compound is characterized by two methylsulfonyl groups attached to the 3rd and 5th positions of the thiazole ring, and a nitrile group (CN) at the 4th position. This molecule is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals due to its unique structure and reactivity. It is typically synthesized through multi-step organic reactions and is used as an intermediate in the preparation of more complex molecules. The compound's properties, such as its solubility and stability, can be influenced by the presence of the methylsulfonyl and nitrile groups, making it a versatile building block in chemical synthesis.

4886-22-0

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4886-22-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4886-22-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,8 and 6 respectively; the second part has 2 digits, 2 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 4886-22:
(6*4)+(5*8)+(4*8)+(3*6)+(2*2)+(1*2)=120
120 % 10 = 0
So 4886-22-0 is a valid CAS Registry Number.

4886-22-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 3,5-bis(methylsulfonyl)-1,2-thiazole-4-carbonitrile

1.2 Other means of identification

Product number -
Other names 3.5-Dimethylsulfonyl-4-cyan-isothiazol

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

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More Details:4886-22-0 SDS

4886-22-0Downstream Products

4886-22-0Relevant academic research and scientific papers

Unusual oxidative dehydration of vic-[alkyl(aryl)thio]-substituted aromatic (heteroaromatic) carboxamides

Kislitsyn,Kucherov,Chukhrov,Zlotin,Starikova,Dolgushin

, p. 916 - 924 (2007/10/03)

A new procedure was developed for the synthesis of nitriles of vic-[alkyl(aryl)sulfonyl] derivatives of benzoic, anthraquinonecarboxylic, and 4-isothiazolecarboxylic acids by the reactions of the corresponding vic-[alkyl(aryl)thio]-substituted aromatic (h

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