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625115-89-1

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625115-89-1 Usage

Structure

A nitrile derivative of indole with a methyl group and a nitro group attached to the indole ring

Usage

Often used as a building block in organic synthesis and pharmaceutical research

Applications

Potential applications in drug and agrochemical development due to unique structural properties and biological activity

Versatility

Used as a reagent in various chemical reactions, making it a valuable compound in organic chemistry.

Check Digit Verification of cas no

The CAS Registry Mumber 625115-89-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,2,5,1,1 and 5 respectively; the second part has 2 digits, 8 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 625115-89:
(8*6)+(7*2)+(6*5)+(5*1)+(4*1)+(3*5)+(2*8)+(1*9)=141
141 % 10 = 1
So 625115-89-1 is a valid CAS Registry Number.

625115-89-1Relevant articles and documents

Selective sodium channel regulator as well as preparation and application thereof

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Paragraph 0228-0233, (2021/02/10)

The invention provides a compound serving as a selective sodium channel regulator and a synthesis and use method, and particularly provides a compound shown as a formula (I), a preparation method of the compound and application of the compound serving as the selective sodium channel regulator. The compounds exhibit excellent activity as a regulator of sodium channels.

NEW SUBSTITUTED ARYLSULPHONYLGLYCINES, THE PREPARATION THEREOF AND THE USE THEREOF AS PHARMACEUTICAL COMPOSITIONS

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, (2008/12/07)

The present invention relates to substituted arylsulphonylglycines of general formula (I) wherein R, X, Y and Z are defined as in claim 1, the tautomers, enantiomers, diastereomers, mixtures thereof and salts thereof, which have valuable pharmacological properties, particularly the suppression of the interaction of glycogen phosphorylase a with the GL subunit of glycogen-associated protein phosphatase 1 (PP1 ), and their use as pharmaceutical compositions.

3-Cyanoindole-based inhibitors of inosine monophosphate dehydrogenase: Synthesis and initial structure-activity relationships

Dhar, T. G. Murali,Shen, Zhongqi,Gu, Henry H.,Chen, Ping,Norris, Derek,Watterson, Scott H.,Ballentine, Shelley K.,Fleener, Catherine A.,Rouleau, Katherine A.,Barrish, Joel C.,Townsend, Robert,Hollenbaugh, Diane L.,Iwanowicz, Edwin J.

, p. 3557 - 3560 (2007/10/03)

A series of novel small molecule inhibitors of inosine monophosphate dehydrogenase (IMPDH), based upon a 3-cyanoindole core, were explored. IMPDH catalyzes the rate determining step in guanine nucleotide biosynthesis and is a target for anticancer, immuno

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