889941-55-3 Usage
Uses
Used in Pharmaceutical Industry:
4-Aminoindole-3-carboxylic acid is used as a key intermediate in the synthesis of various pharmaceuticals. Its unique structure allows for the development of complex molecules with potential therapeutic applications.
Used in Dye Industry:
4-AMINOINDOLE-3-CARBOXYLIC ACID is utilized as a precursor in the production of dyes, contributing to the creation of a wide range of colorants for different industries.
Used in Specialty Chemicals:
4-Aminoindole-3-carboxylic acid serves as a valuable component in the formulation of specialty chemicals, which can be used across various sectors for specific purposes.
Used in Organic Synthesis:
As a building block in organic synthesis, 4-aminoindole-3-carboxylic acid is instrumental in constructing complex organic molecules for research and commercial applications.
Used in Anticancer Research:
4-Aminoindole-3-carboxylic acid has been studied for its potential anticancer properties, making it a candidate for further research and development in oncology.
Used in Antimicrobial Applications:
4-AMINOINDOLE-3-CARBOXYLIC ACID's antimicrobial properties are of interest for potential use in the development of new antimicrobial agents to combat resistant infections.
Check Digit Verification of cas no
The CAS Registry Mumber 889941-55-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,8,9,9,4 and 1 respectively; the second part has 2 digits, 5 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 889941-55:
(8*8)+(7*8)+(6*9)+(5*9)+(4*4)+(3*1)+(2*5)+(1*5)=253
253 % 10 = 3
So 889941-55-3 is a valid CAS Registry Number.
889941-55-3Relevant articles and documents
Synthesis of a Series of Diaminoindoles
Martin, James S.,Mackenzie, Claire J.,Gilbert, Ian H.
, p. 11333 - 11340 (2021)
A selection of 3,4-diaminoindoles were required for a recent drug discovery project. To this end, a 10-step synthesis was developed from 4-nitroindole. This synthesis was subsequently adapted and used to synthesize 3,5-; 3,6-; and 3,7-diaminoindoles from
