Benzamide, 4-amino-N-(2,6-dimethylphenyl)-3-methyl-

Base Information

Chemical Name:Benzamide, 4-amino-N-(2,6-dimethylphenyl)-3-methyl-
CAS No.:109306-93-6
Molecular Formula:C16H18N2O
Molecular Weight:254.332
Hs Code.:
DSSTox Substance ID:DTXSID30431621
Wikidata:Q82245551
ChEMBL ID:CHEMBL47390

Synonyms:109306-93-6;Benzamide, 4-amino-N-(2,6-dimethylphenyl)-3-methyl-;CHEMBL47390;SCHEMBL10401801;DTXSID30431621;AKOS000143098

Suppliers and Price of Benzamide, 4-amino-N-(2,6-dimethylphenyl)-3-methyl-

Supply Marketing:

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

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Chemical Property of Benzamide, 4-amino-N-(2,6-dimethylphenyl)-3-methyl-

Chemical Property:

XLogP3:3.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:254.141913202
Heavy Atom Count:19
Complexity:308

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(C(=CC=C1)C)NC(=O)C2=CC(=C(C=C2)N)C

Technology Process of Benzamide, 4-amino-N-(2,6-dimethylphenyl)-3-methyl-

There total 4 articles about Benzamide, 4-amino-N-(2,6-dimethylphenyl)-3-methyl- 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: 70.0%

: 109306-96-9
3-methyl-4-nitro-N-(2,6-dimethylphenyl)benzamide

: 109306-93-6
4-Amino-N-(2,6-dimethylphenyl)-3-methylbenzamide

Guidance literature:: With hydrogen; palladium on activated charcoal; In ethanol; under 3102.9 Torr;
DOI:10.1021/jm00393a010

Reference yield: 70.0%

: 109306-93-6
4-Amino-N-(2,6-dimethylphenyl)-3-methylbenzamide

Guidance literature:

Reference yield:

: 3113-71-1
3-methyl-4-nitrobenzoic acid

: 109306-93-6
4-Amino-N-(2,6-dimethylphenyl)-3-methylbenzamide

Guidance literature:: Multi-step reaction with 3 steps

1: SOCl₂ / 3 h / Heating

2: Et₃N / tetrahydrofuran / Ambient temperature

3: 70 percent / H₂ / 5percent Pd/C / ethanol / 3102.9 Torr

With thionyl chloride; hydrogen; triethylamine; palladium on activated charcoal; In tetrahydrofuran; ethanol;
DOI:10.1021/jm00393a010