73177-33-0 Usage
Uses
Used in Pharmaceutical Industry:
2-Methyl-1H-indole-6-carboxylic acid is used as a precursor in the synthesis of various pharmaceuticals for its versatile chemical structure and potential biological activities. Its ability to be modified and incorporated into different drug molecules makes it a valuable component in the development of new therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 2-Methyl-1H-indole-6-carboxylic acid is utilized as a starting material for the production of various agrochemicals. Its potential antimicrobial properties can be harnessed to create compounds that protect crops from diseases and pests, thereby increasing agricultural productivity.
Used in Organic Compounds Synthesis:
2-Methyl-1H-indole-6-carboxylic acid serves as a building block in the synthesis of a wide range of organic compounds. Its unique structure allows for the creation of diverse chemical entities that can be applied in various industries, from material science to specialty chemicals.
Used in Medicinal Chemistry Research:
As a compound with potential biological activities, 2-Methyl-1H-indole-6-carboxylic acid is used in medicinal chemistry research to explore its antimicrobial and anticancer properties. This research can lead to the discovery of new drugs and therapies that target specific diseases and conditions.
Used in Drug Development:
In the drug development process, 2-Methyl-1H-indole-6-carboxylic acid is employed as a key intermediate in the synthesis of novel drug candidates. Its chemical properties and potential therapeutic effects make it a promising compound for further investigation and development into effective treatments.
Check Digit Verification of cas no
The CAS Registry Mumber 73177-33-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,3,1,7 and 7 respectively; the second part has 2 digits, 3 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 73177-33:
(7*7)+(6*3)+(5*1)+(4*7)+(3*7)+(2*3)+(1*3)=130
130 % 10 = 0
So 73177-33-0 is a valid CAS Registry Number.
73177-33-0Relevant academic research and scientific papers
Indole and indoline carboxylic acid compounds and method of use
-
, (2008/06/13)
Indole and indoline derivatives of the formula: STR1 wherein indicates a double bond or a single bond between carbon atoms, R1 represents hydrogen, alkyl of 1 through 6 carbon atoms, or alkyl of 1 through 6 carbon atoms substituted by one or more than one of the same type of substituents selected from the hydroxy group, alkenyl groups of 2 through 5 carbon atoms, and alkanoyloxy groups of 2 through 7 carbon atoms, and one of the symbols R2 represents alkyl of 6 through 24 carbon atoms and the other symbol R2 represents alkyl of 1 through 24 carbon atoms or hydrogen, and R3 represents alkyl of 1 through 6 carbon atoms or hydrogen, are new compounds possessing useful pharmacological properties. They are of use in the treatment of diabetes mellitus, hyperlipoproteinaemic states, of atherosclerosis, and of associated conditions.
Indole Synthesis via SRN1 Reactions
Bard, Raymond R.,Bunnett, Joseph F.
, p. 1546 - 1547 (2007/10/02)
o-Haloanilines react with ketone enolate ions in ammonia under irradiation to form indoles in good yields.
