443144-25-0 Usage
Uses
Used in Pharmaceutical Industry:
1H-Indole-7-carboxylic acid, 3-cyanois used as a building block for the synthesis of biologically active molecules due to its unique structural features. The presence of the cyano group at the 3-position of the indole ring allows for the development of new compounds with potential pharmacological properties, making it a promising candidate for drug discovery and development.
Used in Drug Discovery:
1H-Indole-7-carboxylic acid, 3-cyanois utilized as a starting material for the development of new drugs. Its unique structure and potential pharmacological properties make it a valuable asset in the search for novel therapeutic agents. Researchers can modify and optimize its chemical structure to create compounds with improved efficacy, selectivity, and safety profiles for various medical applications.
Used in Medicinal Chemistry Research:
1H-Indole-7-carboxylic acid, 3-cyanoserves as a valuable tool in medicinal chemistry research. Its unique structural features and potential pharmacological properties make it an ideal candidate for studying the structure-activity relationships of biologically active molecules. By investigating the effects of various modifications to its structure, researchers can gain insights into the design of more effective and safer drugs.
Check Digit Verification of cas no
The CAS Registry Mumber 443144-25-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,3,1,4 and 4 respectively; the second part has 2 digits, 2 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 443144-25:
(8*4)+(7*4)+(6*3)+(5*1)+(4*4)+(3*4)+(2*2)+(1*5)=120
120 % 10 = 0
So 443144-25-0 is a valid CAS Registry Number.
443144-25-0Relevant academic research and scientific papers
Process for the preparation of (3-cyano-1h-indol-7-yl) (4-(4-fluorophenethyl) piperazin-1-yl)- methanone and salts thereof
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, (2008/06/13)
The present invention relates to a process for the preparation of(3-cyano-1H-indol-7-yl)[4-(4-fluorophenethyl)piperazin-1-yl]-methanone and salts thereof, characterised in that an indole ester of the formula II in which R is as defined in Claim 1, is conv
