6370-19-0

Basic information

• Product Name: 3-amino-N-(2,4-dimethylphenyl)-4-methylbenzamide
• Synonyms: 3-amino-N-(2,4-dimethylphenyl)-4-methylbenzamide;3-methyl-2',4,4'-trimethylbenzanilide;Einecs 228-877-7;3-AMINO-2',4'-DIMETHYL-P-TOLUANILIDE
• CAS NO: 6370-19-0
• Molecular Formula: C16H18N2O
• Molecular Weight: 254.32692
• EINECS: 228-877-7
• Mol File: 6370-19-0.mol

Chemical Properties

• Boiling Point: 502.7°C at 760 mmHg
• Flash Point: 308.5°C
• Appearance: /
• Density: 1.045g/cm³
• Vapor Pressure: 3.1E-10mmHg at 25°C
• Refractive Index: 1.563
• CAS DataBase Reference: 3-amino-N-(2,4-dimethylphenyl)-4-methylbenzamide(CAS DataBase Reference)
• NIST Chemistry Reference: 3-amino-N-(2,4-dimethylphenyl)-4-methylbenzamide(6370-19-0)
• EPA Substance Registry System: 3-amino-N-(2,4-dimethylphenyl)-4-methylbenzamide(6370-19-0)

Safety Data

• Hazardous Substances Data: 6370-19-0(Hazardous Substances Data)

Usage

Uses

Used in Pharmaceutical Research and Drug Development:
3-amino-N-(2,4-dimethylphenyl)-4-methylbenzamide is used as a research compound for its potential biological activity, which may contribute to the development of new medications for various medical conditions. Its unique structure allows for the possibility of creating derivatives with enhanced properties, making it a promising candidate for the advancement of pharmaceuticals.
Used in the Synthesis of New Pharmaceutical Compounds:
In the field of medicinal chemistry, 3-amino-N-(2,4-dimethylphenyl)-4-methylbenzamide is utilized as a starting material for the synthesis of novel compounds. Its chemical properties enable the creation of modified versions that could possess improved therapeutic effects or reduced side effects, thereby increasing the range of available treatments for different diseases.
Used in the Treatment of Various Medical Conditions:
While further research is necessary to determine the specific applications, 3-amino-N-(2,4-dimethylphenyl)-4-methylbenzamide may have uses in the treatment of a range of medical conditions. Its potential biological activity suggests that it could be a component in the development of new therapies, pending the results of ongoing studies and clinical trials.
Note: The specific applications in different industries or for particular medical conditions have not been detailed in the provided materials. The above uses are inferred based on the general information about the compound's role in pharmaceutical research and development.

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+

Relevant articles and documents

One step diazotization coupling process

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.