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(E)-2-((4-fluorophenyl)sulfonyl)-3-(1H-pyrrol-2-yl)acrylonitrile is a chemical compound characterized by its molecular formula C14H9FN2O2S. It is a sulfonyl-containing acrylonitrile derivative featuring a fluorophenyl group and a pyrrol-2-yl group attached to the acrylonitrile moiety. (E)-2-((4-fluorophenyl)sulfonyl)-3-(1H-pyrrol-2-yl)acrylonitrile is known for its potential applications in pharmaceutical research and organic synthesis.

1313612-96-2

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1313612-96-2 Usage

Uses

Used in Pharmaceutical Research:
(E)-2-((4-fluorophenyl)sulfonyl)-3-(1H-pyrrol-2-yl)acrylonitrile is used as a building block for the synthesis of novel drugs in the pharmaceutical industry. Its unique structure and potential pharmacological activities make it a valuable component in the development of new therapeutic agents.
Used in Organic Synthesis:
In the field of organic chemistry, (E)-2-((4-fluorophenyl)sulfonyl)-3-(1H-pyrrol-2-yl)acrylonitrile serves as a reagent for constructing complex organic molecules. Its versatile chemical properties allow for its use in creating a wide range of compounds with various applications.
Used in Biological Research:
Although further research is required, (E)-2-((4-fluorophenyl)sulfonyl)-3-(1H-pyrrol-2-yl)acrylonitrile has been studied for its potential biological activities and therapeutic applications. Its exploration in this area could lead to the discovery of new treatments for various diseases and conditions.

Check Digit Verification of cas no

The CAS Registry Mumber 1313612-96-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,1,3,6,1 and 2 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1313612-96:
(9*1)+(8*3)+(7*1)+(6*3)+(5*6)+(4*1)+(3*2)+(2*9)+(1*6)=122
122 % 10 = 2
So 1313612-96-2 is a valid CAS Registry Number.

1313612-96-2Relevant academic research and scientific papers

Discovery and optimization of sulfonyl acrylonitriles as selective, covalent inhibitors of protein phosphatase methylesterase-1

Bachovchin, Daniel A.,Zuhl, Andrea M.,Speers, Anna E.,Wolfe, Monique R.,Weerapana, Eranthie,Brown, Steven J.,Rosen, Hugh,Cravatt, Benjamin F.

experimental part, p. 5229 - 5236 (2011/10/09)

The serine hydrolase protein phosphatase methylesterase-1 (PME-1) regulates the methylesterification state of protein phosphatase 2A (PP2A) and has been implicated in cancer and Alzheimer's disease. We recently reported a fluorescence polarization-activit

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