2-{[Methyl(phenyl)amino]carbonyl}benzoic acid

Base Information

• Chemical Name: 2-{[Methyl(phenyl)amino]carbonyl}benzoic acid
• CAS No.: 16931-47-8
• Molecular Formula: C15H13 N O3
• Molecular Weight: 255.27
• Hs Code.: 2924299090
• DSSTox Substance ID: DTXSID10397377
• Wikidata: Q82198665
• Mol file: 16931-47-8.mol

Synonyms:16931-47-8;2-[methyl(phenyl)carbamoyl]benzoic acid;2-{[methyl(phenyl)amino]carbonyl}benzoic acid;2-([Methyl(phenyl)amino]carbonyl)benzoic acid;2-(Methyl(phenyl)carbamoyl)benzoic acid;Oprea1_772756;DTXSID10397377;AKOS000263986;2-(Methyl(phenyl)carbamoyl)benzoicacid;CS-0231327;EN300-10791;Z57127322

Chemical Property of 2-{[Methyl(phenyl)amino]carbonyl}benzoic acid

Chemical Property:

• Vapor Pressure: 4.77E-09mmHg at 25°C
• Boiling Point: 461°Cat760mmHg
• Flash Point: 232.6°C
• PSA: 57.61000
• Density: g/cm³
• LogP: 2.66140
• XLogP3: 1.9
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 3
• Rotatable Bond Count: 3
• Exact Mass: 255.08954328
• Heavy Atom Count: 19
• Complexity: 336

Purity/Quality:

97% ^*data from raw suppliers

2-([METHYL(PHENYL)AMINO]CARBONYL)BENZOIC ACID 95.00% ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CN(C1=CC=CC=C1)C(=O)C2=CC=CC=C2C(=O)O

Technology Process of 2-{[Methyl(phenyl)amino]carbonyl}benzoic acid

There total 1 articles about 2-{[Methyl(phenyl)amino]carbonyl}benzoic acid 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-methylaniline (100-61-8) + o-carboxybenzaldehyde (119-67-5) → N-Methyl-phthalanilinsaeure (16931-47-8)

Guidance literature:

With 1,3-dimethyl-3,4,5,6-tetrahydro-2(1H)-pyrimidinone; [Co(12-TMC)(ACN)](ClO₄)₂; vitamin B₁; C₁₉H₁₅N₂⁽¹⁺⁾*ClO₄^(1-); Fe(EDTA)*H₂O₂; potassium carbonate; potassium hydrogencarbonate; In water; at 20 ℃; for 12h; chemoselective reaction;

DOI:10.1002/cctc.202000156

upstream raw materials:

N-methylaniline

o-carboxybenzaldehyde