63176-44-3 Usage
Uses
Used in Pharmaceutical Industry:
2-METHYL-1H-INDOLE-3-CARBOXYLIC ACID is used as a key intermediate in the synthesis of various pharmaceuticals for its ability to be incorporated into the molecular structures of potential drugs. Its unique chemical properties allow it to contribute to the development of new therapeutic agents.
Used in Agrochemical Industry:
In the agrochemical sector, 2-METHYL-1H-INDOLE-3-CARBOXYLIC ACID is utilized as a building block for the creation of agrochemicals, such as pesticides and herbicides, due to its reactivity and structural features that can be tailored for specific applications in agriculture.
Used in Drug Development:
2-METHYL-1H-INDOLE-3-CARBOXYLIC ACID is employed as a starting material in the development of new drugs, particularly in the areas of anti-inflammatory and anticancer research. Its biological activities make it a promising candidate for further exploration and potential clinical applications.
Used in Medicinal Chemistry Research:
As an important chemical in medicinal chemistry, 2-METHYL-1H-INDOLE-3-CARBOXYLIC ACID is used in research to understand its interactions with biological targets and to optimize its properties for therapeutic use. This includes studying its binding affinity, selectivity, and potential side effects to improve its efficacy and safety profile.
Check Digit Verification of cas no
The CAS Registry Mumber 63176-44-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,3,1,7 and 6 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 63176-44:
(7*6)+(6*3)+(5*1)+(4*7)+(3*6)+(2*4)+(1*4)=123
123 % 10 = 3
So 63176-44-3 is a valid CAS Registry Number.
InChI:InChI=1/C10H9NO2/c1-6-9(10(12)13)7-4-2-3-5-8(7)11-6/h2-5,11H,1H3,(H,12,13)
63176-44-3Relevant academic research and scientific papers
Transformations of phenylhydrazones of dialkyl 2-oxo-propane-1,3- dicarboxylate and of ethyl acetoacetate in concentrated sulfuric acid
Bevk, David,Svete, Jurij,Stanovnik, Branko
, p. 1413 - 1415 (2007/10/03)
The hydrazones 3a,b, prepared from phenylhydrazine (1) and dialkyl 2-oxopropane-1,3-dicarboxylate (2a,b) were converted in concentrated sulfuric acid at -5 °C into a mixture of alkyl (3-carboxyindol-2-yl)acetates (5a,b), and ethyl (5-ethoxy-1-phenyl-1H-pyrazol-3-yl)acetate 6. The hydrazone 8, prepared from 1 and ethyl acetoacetate (7) was transformed under the same conditions into a mixture of five compounds: ethyl 2-methylindol-3-carboxylate (9), 2-methylindol-3-carboxylic acid (10), 2-methylindol (11), 5-ethoxy-3-methyl-1-phenyl-1H-pyrazole (12), and 3-methyl-1-phenyl-1H-pyrazol-5- one (13).
