192991-53-0 Usage
Molecular structure
1H-Indole-3-carboxylic acid, 2-benzoyl-1-(phenylsulfonyl)-, methyl ester is a chemical compound consisting of an indole ring with a carboxylic acid group, a benzoyl group, and a phenylsulfonyl group attached to it.
Esterification
The compound is formed from the esterification of indole-3-carboxylic acid with benzoyl and phenylsulfonyl groups.
Usage
It is commonly used in organic synthesis and pharmaceutical research as a building block for the production of various pharmaceutical drugs and bioactive compounds.
Biological activities
1H-Indole-3-carboxylic acid, 2-benzoyl-1-(phenylsulfonyl)-, methyl ester has demonstrated potential biological activities, such as antitumor and antiviral properties.
Therapeutic effects
The compound has been studied for its therapeutic effects in treating various medical conditions.
Pesticide and herbicide potential
It has been investigated for its potential use as a pesticide and as an herbicide due to its inhibitory effects on plant growth and development.
Check Digit Verification of cas no
The CAS Registry Mumber 192991-53-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,2,9,9 and 1 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 192991-53:
(8*1)+(7*9)+(6*2)+(5*9)+(4*9)+(3*1)+(2*5)+(1*3)=180
180 % 10 = 0
So 192991-53-0 is a valid CAS Registry Number.
192991-53-0Relevant academic research and scientific papers
Fused [d]pyridazin-7-ones
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Page/Page column 13-14, (2008/06/13)
The present invention is directed to fused [d]pyridazin-7-ones. The invention is also directed to methods for making and using the fused [d]pyridazin-7-ones. In particular, the compounds of the present invention may be effective in the treatment of diseases or disease states related to the activity of VEGFR2, MLK1 and CDK5 enzymes, including, for example, angiogenic disorders and neurodegenerative diseases.
Reaction of indole-2,3-dicarboxylic anhydride with grignard reagents: synthesis of 2-acylindoles
Miki, Yasuyoshi
, p. 1143 - 1150 (2007/10/03)
Reaction of indole-2,3-dicarboxylic anhydride with methylmagnesium bromide and phenylmagnesium bromide gave 2-acetyl- and 2-benzoyl-indole-3-carboxylic acids, but with tert-butylmagnesium chloride, 3-pivaloylindole-2-carboxylic acids were obtained as the main products. Treatment of 2-acylindole-3-carboxylic acids with copper chromite in quinoline or potassium hydroxide gave the corresponding 2-acylindoles.
