99-21-8 Usage
Uses
Used in Pharmaceutical Research and Development:
N-(4-AMINO-5-METHOXY-2-METHYLPHENYL)BENZAMIDE is used as a potential drug candidate in pharmaceutical research and development for its potential therapeutic effects in various medical conditions. Its unique chemical structure allows it to interact with biological targets, making it a promising candidate for the treatment of diseases such as cancer and neurological disorders.
Used in the Synthesis of Biologically Active Molecules:
N-(4-AMINO-5-METHOXY-2-METHYLPHENYL)BENZAMIDE is also used as a building block for the synthesis of other biologically active molecules. Its versatile chemical structure can be modified to create new compounds with potential therapeutic properties, expanding the scope of drug discovery and development.
Used in the Chemical Industry:
In the chemical industry, N-(4-AMINO-5-METHOXY-2-METHYLPHENYL)BENZAMIDE may have applications in the synthesis of specialty chemicals and materials. Its unique chemical properties can be leveraged to create novel compounds with specific functions or properties, contributing to the development of new products and technologies.
Check Digit Verification of cas no
The CAS Registry Mumber 99-21-8 includes 5 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 2 digits, 9 and 9 respectively; the second part has 2 digits, 2 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 99-21:
(4*9)+(3*9)+(2*2)+(1*1)=68
68 % 10 = 8
So 99-21-8 is a valid CAS Registry Number.
InChI:InChI=1/C15H16N2O2/c1-10-8-13(16)14(19-2)9-12(10)15(18)17-11-6-4-3-5-7-11/h3-9H,16H2,1-2H3,(H,17,18)
99-21-8Relevant academic research and scientific papers
One step diazotization coupling process
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, (2008/06/13)
A process for producing metal-free azo pigments in purely organic liquid or aqueous/organic liquid containing at most 10% of water calculated on the total weight of the suspension is described. In this one-step process, a suitable aromatic amine is diazotized without isolation of the obtained diazo compound and coupled with a coupling component. Both reactions are carried out in purely or essentially organic medium. The latter consists essentially of such amount of an organic liquid that a substantial portion either of the diazo component or of the coupling component or of both these reactants remain undissolved. Both reactants must be free from sulphonic acid groups. If the resulting azo pigment contains carboxylic acid groups, these can be subsequently converted to the corresponding amido or ester groups.
