Benzamide, N-(2,5-difluorophenyl)-

Base Information

Chemical Name:Benzamide, N-(2,5-difluorophenyl)-
CAS No.:143925-43-3
Molecular Formula:C13H9F2NO
Molecular Weight:233.217
Hs Code.:
DSSTox Substance ID:DTXSID30367855
Nikkaji Number:J503.766B
Wikidata:Q82153985

Synonyms:N-(2,5-difluorophenyl)benzamide;N-[2,5-Difluorophenyl]benzamide;Benzamide, N-(2,5-difluorophenyl)-;143925-43-3;DTXSID30367855;AKOS008555716;(F2_25 or 11-034)

Suppliers and Price of Benzamide, N-(2,5-difluorophenyl)-

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 2 raw suppliers

Chemical Property of Benzamide, N-(2,5-difluorophenyl)-

Chemical Property:

XLogP3:3.4
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:233.06522023
Heavy Atom Count:17
Complexity:266

Purity/Quality:: 99.90% ^*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=C(C=CC(=C2)F)F

Technology Process of Benzamide, N-(2,5-difluorophenyl)-

There total 3 articles about Benzamide, N-(2,5-difluorophenyl)- 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: 95.0%

: 591-50-4
iodobenzene

: 348-54-9
2-Fluoroaniline

: 201230-82-2
carbon monoxide

: 143925-43-3
N-(2,5-difluorophenyl)benzamide

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene; bis-triphenylphosphine-palladium(II) chloride; In N,N-dimethyl acetamide; at 115 ℃; for 3h; under 4912.9 Torr;
DOI:10.1021/jo00049a057

Reference yield:

: 364-74-9
1,4-difluoro-2-nitrobenzene

: 143925-43-3
N-(2,5-difluorophenyl)benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: tin (II)-chloride; aqueous hydrochloric acid

With hydrogenchloride; tin(ll) chloride;