Benzamide, N,N-dibenzoyl-

Base Information

Chemical Name:Benzamide, N,N-dibenzoyl-
CAS No.:602-88-0
Molecular Formula:C21H15NO3
Molecular Weight:329.355
Hs Code.:
NSC Number:16620
DSSTox Substance ID:DTXSID60208949
Nikkaji Number:J138.261F
Wikidata:Q83083095
Mol file:602-88-0.mol

Synonyms:Benzamide, N,N-dibenzoyl-;N,N-dibenzoylbenzamide;Tribenzamide;602-88-0;N,N-Bis(benzoyl)benzamide;Tribenzamid;NSC16620;Benzamide,N-dibenzoyl-;Maybridge4_001837;Oprea1_019838;CBDivE_014410;SCHEMBL1574223;DTXSID60208949;HMS1526D11;NSC 16620;NSC-16620;CCG-238805;NCGC00177206-01;BRD-K42922327-001-01-4

Suppliers and Price of Benzamide, N,N-dibenzoyl-

Supply Marketing:

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 7 raw suppliers

Chemical Property of Benzamide, N,N-dibenzoyl-

Chemical Property:

Vapor Pressure:1.03E-09mmHg at 25°C
Melting Point:206-208 °C
Boiling Point:489.1°Cat760mmHg
PKA:-3.04±0.70(Predicted)
Flash Point:215.2°C
PSA：54.45000
Density:1.249g/cm³
LogP:3.80960
XLogP3:4.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:329.10519334
Heavy Atom Count:25
Complexity:412

Purity/Quality:: 98%min ^*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)N(C(=O)C2=CC=CC=C2)C(=O)C3=CC=CC=C3

Technology Process of Benzamide, N,N-dibenzoyl-

There total 38 articles about Benzamide, N,N-dibenzoyl- 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: 71.0%

: 573-34-2
2,4,5-triphenyloxazole

: 602-88-0
tribenzamide

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; 2,2'-bipyridinium chlorochromate; In dichloromethane; at 0 - 20 ℃; for 2h; Inert atmosphere;
DOI:10.1016/j.tetlet.2017.02.027

Reference yield: 50.0%

: 893-40-3
N-Benzoyl-zimtsaeure-amid

: 98-88-4
benzoyl chloride

: 614-28-8
N-benzoylbenzamide

: 602-88-0
tribenzamide

Guidance literature:: With tributylphosphine; triethylamine; In dichloromethane; at 30 ℃; Inert atmosphere; Schlenk technique;
DOI:10.1021/acs.orglett.9b03116