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1,2-DIMETHYL-1H-IMIDAZOLE-4-SULFONYL CHLORIDE is a chemical compound characterized by its molecular formula C5H8ClNO2S. It is a member of the sulfonamide class and is recognized for its reactivity, particularly due to the chlorine atom present in its structure. 1,2-DIMETHYL-1H-IMIDAZOLE-4-SULFONYL CHLORIDE is instrumental in organic synthesis and pharmaceutical research, where it is utilized to introduce the imidazole-4-sulfonyl chloride group into various molecules, thereby enhancing their biological activity and potential applications in drug and agrochemical development.

137049-02-6

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137049-02-6 Usage

Uses

Used in Pharmaceutical Research and Development:
1,2-DIMETHYL-1H-IMIDAZOLE-4-SULFONYL CHLORIDE is used as a synthetic intermediate for the creation of biologically active compounds. Its ability to introduce the imidazole-4-sulfonyl chloride group is crucial for the development of new drugs with potential therapeutic applications.
Used in Agrochemical Development:
In the agrochemical industry, 1,2-DIMETHYL-1H-IMIDAZOLE-4-SULFONYL CHLORIDE is used as a key component in the synthesis of compounds with pesticidal properties. The imidazole-4-sulfonyl chloride group it introduces can enhance the effectiveness of agrochemicals in controlling pests and diseases in agriculture.
Used in Organic Synthesis:
1,2-DIMETHYL-1H-IMIDAZOLE-4-SULFONYL CHLORIDE serves as a versatile reagent in organic synthesis, where it is employed to modify the structure of organic compounds. This modification can lead to the creation of new molecules with improved or novel properties, expanding the scope of chemical research and applications.
Safety Precautions:
Due to the reactivity of 1,2-DIMETHYL-1H-IMIDAZOLE-4-SULFONYL CHLORIDE, it is essential to handle 1,2-DIMETHYL-1H-IMIDAZOLE-4-SULFONYL CHLORIDE with care. Appropriate safety measures, including the use of personal protective equipment and adherence to laboratory safety protocols, must be followed to minimize risks associated with its use.

Check Digit Verification of cas no

The CAS Registry Mumber 137049-02-6 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,7,0,4 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 137049-02:
(8*1)+(7*3)+(6*7)+(5*0)+(4*4)+(3*9)+(2*0)+(1*2)=116
116 % 10 = 6
So 137049-02-6 is a valid CAS Registry Number.
InChI:InChI=1/C5H7ClN2O2S/c1-4-7-5(3-8(4)2)11(6,9)10/h3H,1-2H3

137049-02-6SDS

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 1,2-dimethylimidazole-4-sulfonyl chloride

1.2 Other means of identification

Product number -
Other names 1,2-Dimethyl-1H-imidazole-4-sulfonyl chloride

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:137049-02-6 SDS

137049-02-6Upstream product

137049-02-6Relevant articles and documents

ALKYLAMINOPYRIDINE DERIVATIVE

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Page/Page column 49; 50, (2011/01/11)

The present invention relates to a compound that is useful for treatment of, for example, hypertension, arteriosclerosis, bulimia and obesity because of having an antagonistic action to a neuropeptide Y receptor and is represented by formula (I) [wherein R1 represents hydrogen, cyano, or the like; R represents a group represented by formula (II); X1 represents C1-4 lower alkylene or the like; X2 represents lower alkylene or the like; and Het represents a 5-membered heteroaromatic ring that has at least one nitrogen atom and, in addition, one or two hetero atoms selected from the group consisting of nitrogen, sulfur and oxygen atoms] or to a pharmaceutically acceptable salt thereof.

Syntheses of 2-(2-arylethyl)imidazoles

Shafiee,Rastkary,Foroumadi

, p. 607 - 610 (2007/10/03)

Condensation of 2-methylimidazole with arylaldehyde 4 and subsequent reduction of the intermediate 5 with Raney-nickel gave 2-[2-(2,4- dichlorophenyl)ethyl]imidazole 2. Compound 11 was prepared from compound 10 similarly. Reaction of compound 2 with methy

Imidazole compounds, processes for their preparation, pharmaceuticals based on these compounds and some intermediates

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, (2008/06/13)

Imidazole compounds of the formula I STR1 in which R1 =alkyl, R2 and R3 =H, halogen or alkyl, X=OH or an amide radical having certain substituents, processes for their preparation and pharmaceuticals based on these compounds, in particular for the prophylaxis and treatment of circulatory disturbances, especially of disturbances of the microcirculation and of the disorders resulting therefrom, and some novel intermediates for the preparation of the compounds of the formula I, which are 1-methyl-, 1,2-dimethyl- and 1-ethyl-4-imidazolesulfonyl chloride.

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