n-(3-Fluorophenyl)benzamide

Base Information

Chemical Name:n-(3-Fluorophenyl)benzamide
CAS No.:1629-15-8
Molecular Formula:C13H10 F N O
Molecular Weight:215.227
Hs Code.:
NSC Number:51887
DSSTox Substance ID:DTXSID00936759
Nikkaji Number:J881.950E
Wikidata:Q27213029
ChEMBL ID:CHEMBL1451503
Mol file:1629-15-8.mol

Synonyms:n-(3-fluorophenyl)benzamide;1629-15-8;N-(3-Fluoro-phenyl)-benzamide;NSC51887;MLS000523639;CHEMBL1451503;SCHEMBL23447715;Benzamide, N-(3-fluorophenyl)-;DTXSID00936759;CHEBI:123320;KOUNOYCEOGJXJH-UHFFFAOYSA-N;HMS2380L06;NSC-51887;STL289946;AKOS000592633;N-Benzoyl derivative of m-fluoroaniline;SMR000122712;N-(3-Fluorophenyl)benzenecarboximidic acid;Q27213029;Z28143197

Suppliers and Price of n-(3-Fluorophenyl)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 7 raw suppliers

Chemical Property of n-(3-Fluorophenyl)benzamide

Chemical Property:

Vapor Pressure:0.0327mmHg at 25°C
Boiling Point:243.1°C at 760 mmHg
Flash Point:100.8°C
Density:1.247g/cm³
XLogP3:2.7
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:215.074642105
Heavy Atom Count:16
Complexity:238

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=C2)F

Technology Process of n-(3-Fluorophenyl)benzamide

There total 12 articles about n-(3-Fluorophenyl)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%

: 768-35-4
3-fluorophenylboronic acid

: 19226-36-9
3-phenyl-5H-1,4,2-dioxazol-5-one

: 1629-15-8
N-(3-fluorophenyl)benzamide

Guidance literature:: With iron(II) chloride; In 1,2-dichloro-ethane; at 40 ℃; for 16h; chemoselective reaction; Inert atmosphere; Irradiation;
DOI:10.1021/acscatal.1c04538