3-amino-N-(2-methylphenyl)benzamide

Base Information

• Chemical Name: 3-amino-N-(2-methylphenyl)benzamide
• CAS No.: 14315-20-9
• Molecular Formula: C14H14N2O
• Molecular Weight: 226.27
• Hs Code.: 2924299090
• DSSTox Substance ID: DTXSID00396117
• Wikidata: Q82196649
• ChEMBL ID: CHEMBL289261
• Mol file: 14315-20-9.mol

Synonyms:3-amino-N-(2-methylphenyl)benzamide;14315-20-9;3-Amino-N-(o-tolyl)benzamide;Oprea1_842764;3-Amino-N-o-tolyl-benzamide;CHEMBL289261;SCHEMBL21870336;DTXSID00396117;BBL002448;MFCD00440152;STK267596;AKOS000150017;SB80153;3-amino-N~1~-(2-methylphenyl)benzamide;VS-01078;CS-0314264

Chemical Property of 3-amino-N-(2-methylphenyl)benzamide

Chemical Property:

• Vapor Pressure: 0.000135mmHg at 25°C
• Boiling Point: 333.6°C at 760 mmHg
• Flash Point: 155.5°C
• PSA: 55.12000
• Density: 1.21g/cm³
• LogP: 3.48370
• XLogP3: 2.1
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 2
• Exact Mass: 226.110613074
• Heavy Atom Count: 17
• Complexity: 267

Purity/Quality:

99% ^*data from raw suppliers

3-Amino-N-(2-methylphenyl)benzamide ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=CC=CC=C1NC(=O)C2=CC(=CC=C2)N

Technology Process of 3-amino-N-(2-methylphenyl)benzamide

There total 4 articles about 3-amino-N-(2-methylphenyl)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: 67.0%

3-nitro-benzoic acid o-toluidide (102631-02-7) → 3-Amino-benz-o-toluidid (14315-20-9)

Guidance literature:

With hydrogen; palladium on activated charcoal; for 3h; under 2327.2 Torr;

DOI:10.1021/jm00158a038

Reference yield:

o-toluidine (95-53-4) → 3-Amino-benz-o-toluidid (14315-20-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 85 percent / aq. K₂CO₃ / tetrahydrofuran / 12 h / Heating

2: 67 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:

m-nitrobenzoic acid chloride (121-90-4) → 3-Amino-benz-o-toluidid (14315-20-9)

Guidance literature:

Multi-step reaction with 2 steps

1: 85 percent / aq. K₂CO₃ / tetrahydrofuran / 12 h / Heating

2: 67 percent / H₂ / 5percent Pd/C / 3 h / 2327.2 Torr

With hydrogen; potassium carbonate; palladium on activated charcoal; In tetrahydrofuran;

DOI:10.1021/jm00158a038

upstream raw materials:

3-nitro-benzoic acid o-toluidide

o-toluidine

m-nitrobenzoic acid chloride

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