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50790-30-2

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50790-30-2 Usage

General Description

N-(3-Cyanophenyl)methanesulfonamide is a chemical compound with the formula C8H8N2O2S. It is a white solid that is soluble in organic solvents but insoluble in water. N-(3-CYANOPHENYL)METHANESULFONAMIDE is commonly used as a reagent in organic synthesis, particularly in the formation and modification of carbon-carbon and carbon-nitrogen bonds. It is also employed in the pharmaceutical industry as a building block for the synthesis of various pharmaceutical compounds. Additionally, N-(3-Cyanophenyl)methanesulfonamide has been studied for its potential biological activities, including its antimicrobial and antitumor properties, making it a subject of interest in medicinal chemistry research.

Check Digit Verification of cas no

The CAS Registry Mumber 50790-30-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,0,7,9 and 0 respectively; the second part has 2 digits, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 50790-30:
(7*5)+(6*0)+(5*7)+(4*9)+(3*0)+(2*3)+(1*0)=112
112 % 10 = 2
So 50790-30-2 is a valid CAS Registry Number.
InChI:InChI=1/C8H8N2O2S/c1-13(11,12)10-8-4-2-3-7(5-8)6-9/h2-5,10H,1H3

50790-30-2Relevant articles and documents

BIFUNCTIONAL SUBSTITUED PYRIMIDINES AS MODULATORS OF FAK PROTEOLYSE

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Paragraph 00408, (2020/02/16)

The present disclosure relates to bifunctional compounds, which find utility as modulators of focal adhesion kinase (FAK) or protein tyrosine kinase 2 (PTK2). In particular, the present disclosure is directed to bifunctional compounds, which contain on one end a Von Hippel-Lindau, cereblon, Inhibitors of Apotosis Proteins or mouse double-minute homolog 2 ligand which binds to the respective E3 ubiquitin ligase and on the other end a moiety which binds the target protein, such that the target protein is placed in proximity to the ubiquitin ligase to effect degradation (and inhibition) of target protein. The present disclosure exhibits a broad range of pharmacological activities associated with degradation/inhibition of target protein. Diseases or disorders that result from aggregation or accumulation of the target protein are treated or prevented with compounds and compositions of the present disclosure.

HETEROARYL-PYRAZOLE DERIVATIVE

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Paragraph 0494; 0495; 0496; 0497; 0498, (2013/06/05)

A compound represented by formula [I] and a pharmaceutically accepted salt of said compound are a novel compound and a pharmaceutically accepted salt thereof which exert antagonistic activity against group II metabotropic glutamate (mGlu) receptors, and are effective as a novel preventive or therapeutic agent for disorders such as mood disorders (depressive disorder, bipolar disorder, etc.), anxiety disorders (generalized anxiety disorder, panic disorder, obsessive-compulsive disorder, social anxiety disorder, posttraumatic stress disorder, a specific phobic disorder, acute stress disorder, etc.), schizophrenia, Alzheimer's disease, cognitive impairment, dementia, drug dependence, convulsions, shivering, pain, sleep disorders, and the like.

SULFONYL AMIDE DERIVATIVES FOR THE TREATMENT OF ABNORMAL CELL GROWTH

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Page/Page column 35, (2009/04/24)

The present invention relates to a compound of the formula I wherein R1 to R6, A, B, n and m are as defined herein. Such novel sulfonyl amide derivatives are useful in the treatment of abnormal cell growth, such as cancer, in mammals. This invention also relates to a method of using such compounds in the treatment of abnormal cell growth in mammals, especially humans, and to pharmaceutical compositions containing such compounds.

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