99-21-8 Usage
General Description
N-(4-AMINO-5-METHOXY-2-METHYLPHENYL)BENZAMIDE is a chemical compound with the molecular formula C15H15N2O2. It belongs to the class of organic compounds known as benzamides. N-(4-AMINO-5-METHOXY-2-METHYLPHENYL)BENZAMIDE is primarily used in pharmaceutical research and development as a potential drug candidate or as a building block for the synthesis of other biologically active molecules. It has been studied for its potential therapeutic effects in various medical conditions, including cancer and neurological disorders. Additionally, it may also have industrial applications in the synthesis of specialty chemicals and materials. However, further research is needed to fully understand its properties and potential applications.
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 articles and documents
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.
