3-Amino-N-[2-methyl-6-(1-methylethyl)phenyl]benzamide

Base Information

Chemical Name:3-Amino-N-[2-methyl-6-(1-methylethyl)phenyl]benzamide
CAS No.:102630-92-2
Molecular Formula:C₁₇H₂₀N₂O
Molecular Weight:268.359
Hs Code.:
ChEMBL ID:CHEMBL39788
DSSTox Substance ID:DTXSID701215302

Synonyms:102630-92-2;CHEMBL39788;3-Amino-N-[2-methyl-6-(1-methylethyl)phenyl]benzamide;DTXSID701215302;AKOS000160727

Suppliers and Price of 3-Amino-N-[2-methyl-6-(1-methylethyl)phenyl]benzamide

Supply Marketing:

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

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Chemical Property of 3-Amino-N-[2-methyl-6-(1-methylethyl)phenyl]benzamide

Chemical Property:

XLogP3:3.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:3
Exact Mass:268.157563266
Heavy Atom Count:20
Complexity:329

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

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

Technology Process of 3-Amino-N-[2-methyl-6-(1-methylethyl)phenyl]benzamide

There total 3 articles about 3-Amino-N-[2-methyl-6-(1-methylethyl)phenyl]benzamide 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: 57.0%

: 102631-10-7
N-(2-Isopropyl-6-methyl-phenyl)-3-nitro-benzamide

: 102630-92-2
3-Amino-N-(2-isopropyl-6-methyl-phenyl)-benzamide

Guidance literature:: With hydrogen; palladium on activated charcoal; for 3h; under 2327.2 Torr;
DOI:10.1021/jm00158a038

Reference yield:

: 5266-85-3
2-isopropyl-6-methylaniline

: 102630-92-2
3-Amino-N-(2-isopropyl-6-methyl-phenyl)-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / aq. K₂CO₃ / tetrahydrofuran / 12 h / Heating

2: 57 percent / H₂ / 5percent Pd/C / 3 h / 2327.2 Torr

With hydrogen; potassium carbonate; palladium on activated charcoal; In tetrahydrofuran;
DOI:10.1021/jm00158a038

Reference yield:

: 121-90-4
m-nitrobenzoic acid chloride

: 102630-92-2
3-Amino-N-(2-isopropyl-6-methyl-phenyl)-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / aq. K₂CO₃ / tetrahydrofuran / 12 h / Heating

2: 57 percent / H₂ / 5percent Pd/C / 3 h / 2327.2 Torr

With hydrogen; potassium carbonate; palladium on activated charcoal; In tetrahydrofuran;
DOI:10.1021/jm00158a038