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5-(Dimethylsulfamoyl)thiophene-2-carboxylic acid is a chemical compound with the molecular formula C7H9NO2S2. It is a derivative of thiophene, a heterocyclic compound consisting of a benzene ring with one sulfur atom replacing one carbon atom. The molecule features a dimethylsulfamoyl group (-S(=O)(=O)N(CH3)2) attached to the 5-position of the thiophene ring and a carboxylic acid group (-COOH) at the 2-position. 5-(dimethylsulfamoyl)thiophene-2-carboxylic acid is known for its potential applications in the synthesis of various pharmaceuticals and agrochemicals, as well as its use as an intermediate in the production of other organic compounds. Its chemical structure and properties make it a versatile building block in organic synthesis, particularly in the development of sulfur-containing compounds with diverse biological activities.

7311-36-6

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7311-36-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7311-36-6 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,3,1 and 1 respectively; the second part has 2 digits, 3 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7311-36:
(6*7)+(5*3)+(4*1)+(3*1)+(2*3)+(1*6)=76
76 % 10 = 6
So 7311-36-6 is a valid CAS Registry Number.

7311-36-6Relevant academic research and scientific papers

KCNT1 INHIBITORS AND METHODS OF USE

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Paragraph 000204, (2020/11/23)

The present invention is directed to, in part, compounds and compositions useful for preventing and/or treating a neurological disease or disorder, a disease or condition relating to excessive neuronal excitability, and/or a gain-of-function mutation in a gene (e.g., KCNT1). Methods of treating a neurological disease or disorder, a disease or condition relating to excessive neuronal excitability, and/or a gain-of-function mutation in a gene such as KCNT1 are also provided herein.

COMPOUNDS AND USES THEREOF

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Page/Page column 141-142, (2019/08/26)

The present disclosure features compounds useful for the treatment of BAF complex-related disorders.

3-SUBSTITUTED-2-OXINDOLE DERIVATIVES

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, (2008/06/13)

This invention relates to novel 3-substituted-2-oxindole derivatives which are inhibitors of prostaglandin H 2 synthase, 5-lipoxygenase and interleukin-1 biosynthesis. The compounds of the invention are useful as inhibitors of prostaglandin H 2 synthase and interleukin-1 biosynthesis, per se, and as analgesic, antiinflammatory and antiarthritic agents in the treatment of chronic inflammatory diseases. This invention also relates to pharmaceutical compositions comprising said 3-substituted-2-oxindole derivatives; to methods of inhibiting prostaglandin H 2 synthase and biosynthesis of interleukin-1; and to treating chronic inflammatory diseases in a mammal with said compounds. Further, this invention relates to certain novel carboxylic acids useful as intermediates in the preparation of the 3-substituted-2-oxindole derivatives of this invention and to a process for the preparation of the 3-substituted-2-oxindole derivatives.

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