3-amino-N-ethyl-4-methylbenzamide

Base Information

Chemical Name:3-amino-N-ethyl-4-methylbenzamide
CAS No.:29526-66-7
Molecular Formula:C₁₀H₁₄N₂O
Molecular Weight:178.234
Hs Code.:
European Community (EC) Number:965-200-0

Synonyms:3-amino-N-ethyl-4-methylbenzamide;29526-66-7;SCHEMBL3250190;XPBQHLXMYVRYSO-UHFFFAOYSA-N;3-Amino-N-ethyl-4-methyl-benzamide;AKOS000113271;CS-0118567;EN300-42064;Z239124824

Suppliers and Price of 3-amino-N-ethyl-4-methylbenzamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 3 raw suppliers

Chemical Property of 3-amino-N-ethyl-4-methylbenzamide

Chemical Property:

XLogP3:0.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:178.110613074
Heavy Atom Count:13
Complexity:182

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCNC(=O)C1=CC(=C(C=C1)C)N

Technology Process of 3-amino-N-ethyl-4-methylbenzamide

There total 2 articles about 3-amino-N-ethyl-4-methylbenzamide which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield:

: 75-04-7,85404-22-4
ethylamine

: 10397-30-5
4-methyl-3-nitrobenzoyl chloride

: 29526-66-7
N-ethyl-3-amino-4-methylbenzamide

Guidance literature:: In tetrahydrofuran; 4-(dicyanomethylene)-2-methyl-6-(p-dimethylaminostyryl)-4H-pyran;

Reference yield:

: 10397-30-5
4-methyl-3-nitrobenzoyl chloride

: 29526-66-7
N-ethyl-3-amino-4-methylbenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: triethylamine / dichloromethane / 20 °C

2: palladium 10% on activated carbon; hydrogen / ethanol / 20 °C

With palladium 10% on activated carbon; hydrogen; triethylamine; In ethanol; dichloromethane;
DOI:10.1016/j.bmcl.2012.04.116

Reference yield:

: 54045-76-0
2-bromo-thiazole-5-carboxylic acid

: 29526-66-7
N-ethyl-3-amino-4-methylbenzamide

: C₁₄H₁₄BrN₃O₂S

Guidance literature:: With benzotriazol-1-ol; N-(3-dimethylaminopropyl)-N-ethylcarbodiimide; N-ethyl-N,N-diisopropylamine; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1016/j.bmcl.2008.02.031