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

Base Information

Chemical Name:N-(2-Bromo-4-methylphenyl)benzamide
CAS No.:77791-07-2
Molecular Formula:C14H12BrNO
Molecular Weight:290.159
Hs Code.:
DSSTox Substance ID:DTXSID30357418
Nikkaji Number:J1.642.818C
Wikidata:Q82137311

Synonyms:N-(2-Bromo-4-methylphenyl)benzamide;77791-07-2;Benzamide, N-(2-bromo-4-methylphenyl)-;DTXSID30357418;AKOS000190872;A1-04935

Suppliers and Price of N-(2-Bromo-4-methylphenyl)benzamide

Supply Marketing:

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

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

Chemical Property:

Vapor Pressure:0.000662mmHg at 25°C
XLogP3:4.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:289.01023
Heavy Atom Count:17
Complexity:263

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

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

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

There total 18 articles about N-(2-Bromo-4-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: 98.0%

2-bromo-p-toluidine: 583-68-6
2-bromo-p-toluidine

: 98-88-4
benzoyl chloride

: 77791-07-2
N-(2-bromo-4-methylphenyl)-benzamide

Guidance literature:: In tetrahydrofuran; at 20 ℃; for 24h;
DOI:10.1021/jo051927q

Reference yield: 90.0%

: 582-78-5
N-(4-methylphenyl)benzamide

: 77791-07-2
N-(2-bromo-4-methylphenyl)-benzamide

Guidance literature:: With hydrogen bromide; Selectfluor; In water; at 20 ℃; for 4h; regioselective reaction;
DOI:10.1016/j.tetlet.2016.10.092