4-amino-N-(4-amino-2-methylphenyl)benzamide

Base Information

• Chemical Name: 4-amino-N-(4-amino-2-methylphenyl)benzamide
• CAS No.: 14303-59-4
• Molecular Formula: C14H15N3O
• Molecular Weight: 241.293
• DSSTox Substance ID: DTXSID20405371
• Nikkaji Number: J912.276A
• Mol file: 14303-59-4.mol

Synonyms:4-amino-N-(4-amino-2-methylphenyl)benzamide;14303-59-4;Benzamide, 4-amino-N-(4-amino-2-methylphenyl)-;Oprea1_550760;SCHEMBL3880896;DTXSID20405371;YCSQADLXNHJXCN-UHFFFAOYSA-N;4,4'-diamino-2'-methyl-benzanilide;AKOS001483309;EU-0000107;SR-01000389392;SR-01000389392-1

Chemical Property of 4-amino-N-(4-amino-2-methylphenyl)benzamide

Chemical Property:

• XLogP3: 1.6
• Hydrogen Bond Donor Count: 3
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 241.121512110
• Heavy Atom Count: 18
• Complexity: 287

Purity/Quality:

99.90% ^*data from raw suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

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

Technology Process of 4-amino-N-(4-amino-2-methylphenyl)benzamide

There total 3 articles about 4-amino-N-(4-amino-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: 75.0%

N-(2-methyl-4-nitrophenyl)-4-nitrobenzamide → 4-amino-N-(4-amino-2-methylphenyl)benzamide (14303-59-4)

Guidance literature:

With hydrogen; cyclohexene; palladium on activated charcoal; In isopropyl alcohol; for 8h; Heating;

DOI:10.1111/j.1600-0773.1998.tb01397.x

Reference yield:

2-methyl-4-nitro-benzenamine (99-52-5) → 4-amino-N-(4-amino-2-methylphenyl)benzamide (14303-59-4)

Guidance literature:

Multi-step reaction with 2 steps

1: 87 percent / pyridine

2: 75 percent / H₂; cyclohexene / Pd/C / propan-2-ol / 8 h / Heating

With pyridine; hydrogen; cyclohexene; palladium on activated charcoal; In isopropyl alcohol;

DOI:10.1111/j.1600-0773.1998.tb01397.x

Reference yield:

4-nitro-benzoyl chloride (122-04-3) → 4-amino-N-(4-amino-2-methylphenyl)benzamide (14303-59-4)

Guidance literature:

Multi-step reaction with 2 steps

1: 87 percent / pyridine

2: 75 percent / H₂; cyclohexene / Pd/C / propan-2-ol / 8 h / Heating

With pyridine; hydrogen; cyclohexene; palladium on activated charcoal; In isopropyl alcohol;

DOI:10.1111/j.1600-0773.1998.tb01397.x

upstream raw materials:

4-nitro-benzoyl chloride

2-methyl-4-nitro-benzenamine