6370-19-0 Usage
General Description
3-amino-N-(2,4-dimethylphenyl)-4-methylbenzamide is a chemical compound with the molecular formula C16H18N2O. It is an amide derivative of benzamide, containing an amino group and two methyl groups on the phenyl ring. 3-amino-N-(2,4-dimethylphenyl)-4-methylbenzamide is commonly used in pharmaceutical research and drug development due to its potential biological activity. It may have applications in the treatment of various medical conditions, and its chemical structure makes it a valuable target for synthesis and modification to create new pharmaceutical compounds with enhanced properties. Further research is needed to fully understand the potential uses and effects of 3-amino-N-(2,4-dimethylphenyl)-4-methylbenzamide.
Check Digit Verification of cas no
The CAS Registry Mumber 6370-19-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,7 and 0 respectively; the second part has 2 digits, 1 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6370-19:
(6*6)+(5*3)+(4*7)+(3*0)+(2*1)+(1*9)=90
90 % 10 = 0
So 6370-19-0 is a valid CAS Registry Number.
InChI:InChI=1/C22H29NO/c1-16-13-14-18(15-17(16)2)23-22(24)21-19-11-9-7-5-3-4-6-8-10-12-20(19)21/h5-8,13-15,19-21H,3-4,9-12H2,1-2H3,(H,23,24)/b7-5-,8-6+
6370-19-0Relevant 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.
