N-(2-benzamidophenyl)benzamide

Base Information Edit

Chemical Name:N-(2-benzamidophenyl)benzamide
CAS No.:744-38-7
Molecular Formula:C20H16N2O2
Molecular Weight:316.359
Hs Code.:
European Community (EC) Number:662-741-1
NSC Number:81574,28628
DSSTox Substance ID:DTXSID30282897
Nikkaji Number:J79.932G
Wikidata:Q82017286
ChEMBL ID:CHEMBL44839
Mol file:744-38-7.mol

Synonyms:N-(2-benzamidophenyl)benzamide;744-38-7;N,N'-(o-Phenylene)bisbenzamide;CHEMBL44839;N,N'-(1,2-Phenylene)dibenzamide;Benzamide,N'-1,2-phenylenebis-;NSC81574;Benzamide, N,N'-1,2-phenylenebis-;Cambridge id 5140043;NCIOpen2_009086;Oprea1_489566;SCHEMBL1110180;DTXSID30282897;N,N'-dibenzoyl-o-phenylenediamine;PDRZOLRKTPJCNY-UHFFFAOYSA-N;NSC28628;BDBM50142508;N-(2-Benzoylamino-phenyl)-benzamide;NSC-28628;NSC-81574;AKOS001012034;N-[2-(Benzoylamino)phenyl]benzamide #;N-(2-(BENZOYLAMINO)PHENYL)BENZAMIDE;CS-0289938;EU-0002139;SR-01000405395;SR-01000405395-1;Z56788102

Suppliers and Price of N-(2-benzamidophenyl)benzamide

Supply Marketing:Edit

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 4 raw suppliers

Chemical Property of N-(2-benzamidophenyl)benzamide Edit

Chemical Property:

Boiling Point:358.2°Cat760mmHg
Flash Point:103.8°C
PSA：58.20000
Density:1.279g/cm³
LogP:4.33720
XLogP3:3.5
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:316.121177757
Heavy Atom Count:24
Complexity:385

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C(=O)NC2=CC=CC=C2NC(=O)C3=CC=CC=C3

Technology Process of N-(2-benzamidophenyl)benzamide

There total 34 articles about N-(2-benzamidophenyl)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: 99.0%

: 98-88-4
benzoyl chloride

: 95-54-5
1,2-diamino-benzene

: 744-38-7
1,2-dibenzamidobenzene

Guidance literature:: With pyridine; In tetrahydrofuran;
DOI:10.1039/a802123f

Reference yield: 96.0%

: 591-50-4
iodobenzene

: 201230-82-2
carbon monoxide

: 95-54-5
1,2-diamino-benzene

: 744-38-7
1,2-dibenzamidobenzene

: 716-79-0
2-phenyl-1H-benzoimidazole

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene; bis(triphenylphosphine)palladium(II)-chloride; In N,N-dimethyl acetamide; at 145 ℃; for 2.5h; under 4912.9 Torr;
DOI:10.1021/jo00077a019