N-(4-bromo-2-phenylphenyl)benzamide

Base Information

Chemical Name:N-(4-bromo-2-phenylphenyl)benzamide
CAS No.:7511-41-3
Molecular Formula:C19H14 Br N O
Molecular Weight:352.2246
Hs Code.:
NSC Number:51000
DSSTox Substance ID:DTXSID70996608
Wikidata:Q82988440

Synonyms:7511-41-3;NSC51000;DTXSID70996608;NSC-51000;N-(5-Bromo[1,1'-biphenyl]-2-yl)benzenecarboximidic acid

Suppliers and Price of N-(4-bromo-2-phenylphenyl)benzamide

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 6 raw suppliers

Chemical Property of N-(4-bromo-2-phenylphenyl)benzamide

Chemical Property:

Vapor Pressure:1.44E-06mmHg at 25°C
Boiling Point:398.8°C at 760 mmHg
Flash Point:195°C
Density:1.41g/cm³
XLogP3:4.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:3
Exact Mass:351.02588
Heavy Atom Count:22
Complexity:360

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)C2=C(C=CC(=C2)Br)NC(=O)C3=CC=CC=C3

Technology Process of N-(4-bromo-2-phenylphenyl)benzamide

There total 8 articles about N-(4-bromo-2-phenylphenyl)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: 50.0%

: 5455-13-0
2-amino-5-bromobiphenyl

: 98-88-4
benzoyl chloride

: 7511-41-3
2-benzamido-5-bromobiphenyl

Guidance literature:: With triethylamine; In ethyl acetate; at 20 ℃;
DOI:10.1002/chem.202003430

Reference yield:

: 86-00-0
2-nitrobiphenyl

: 7511-41-3
2-benzamido-5-bromobiphenyl

Guidance literature:: Multi-step reaction with 5 steps

1: tin; hydrochloric acid

2: 0 °C

3: glacial acetic acid; bromine

4: alcoholic hydrobromic acid / Hydrolysis

5: durch Benzoylierung

With hydrogenchloride; tin; hydrogen bromide; bromine; acetic acid;

Reference yield:

: 90-41-5
2-phenylaniline

: 7511-41-3
2-benzamido-5-bromobiphenyl

Guidance literature:: Multi-step reaction with 4 steps

1: 0 °C

2: glacial acetic acid; bromine

3: alcoholic hydrobromic acid / Hydrolysis

4: durch Benzoylierung

With hydrogen bromide; bromine; acetic acid;