N-(4-bromo-3-methylphenyl)-3-nitrobenzamide

Base Information

• Chemical Name: N-(4-bromo-3-methylphenyl)-3-nitrobenzamide
• CAS No.: 62129-28-6
• Molecular Formula: C14H11BrN2O3
• Molecular Weight: 335.15300
• DSSTox Substance ID: DTXSID70358929
• Wikidata: Q82139856
• Mol file: 62129-28-6.mol

Synonyms:N-(4-bromo-3-methylphenyl)-3-nitrobenzamide;STK066766;62129-28-6;DTXSID70358929;AKOS000187920;Z30826455

Chemical Property of N-(4-bromo-3-methylphenyl)-3-nitrobenzamide

Chemical Property:

• PSA: 74.92000
• LogP: 4.51420
• XLogP3: 4.3
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 2
• Exact Mass: 333.99530
• Heavy Atom Count: 20
• Complexity: 372

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=C(C=CC(=C1)NC(=O)C2=CC(=CC=C2)[N+](=O)[O-])Br

Technology Process of N-(4-bromo-3-methylphenyl)-3-nitrobenzamide

There total 1 articles about N-(4-bromo-3-methylphenyl)-3-nitrobenzamide 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: 72.0%

amino-5-bromo-2-toluene (6933-10-4) + 3-nitrobenzoic acid (121-92-6) → N-(4-bromo-3-methylphenyl)-3-nitrobenzamide (62129-28-6)

Guidance literature:

With O-(benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborate; N-ethyl-N,N-diisopropylamine; In dichloromethane; at 0 - 20 ℃; for 3h;

DOI:10.1021/acs.jmedchem.6b01180

Reference yield: 78.0%

N-(4-bromo-3-methylphenyl)-3-nitrobenzamide (62129-28-6) → 3-amino-N-(4-bromo-3-methylphenyl)benzamide

Guidance literature:

With tin(II) chloride dihdyrate; In ethanol; at 75 ℃; for 2.5h;

DOI:10.1021/acs.jmedchem.6b01180

upstream raw materials:

amino-5-bromo-2-toluene

3-nitrobenzoic acid