Benzamide, 2,6-difluoro-N-((phenylamino)carbonyl)-

Base Information

Chemical Name:Benzamide, 2,6-difluoro-N-((phenylamino)carbonyl)-
CAS No.:57160-53-9
Molecular Formula:C14H10F2N2O2
Molecular Weight:276.2382
Hs Code.:
DSSTox Substance ID:DTXSID60205796
Nikkaji Number:J481.178J
Wikidata:Q83079467

Synonyms:2,6-difluoro-N-((phenylamino)carbonyl)benzamide;57160-53-9;Benzamide, 2,6-difluoro-N-((phenylamino)carbonyl)-;DTXSID60205796;1-(2,6-Difluorobenzoyl)-3-[phenyl]urea;2,6-difluoro-N-(phenyl-carbamoyl)-benzamide

Suppliers and Price of Benzamide, 2,6-difluoro-N-((phenylamino)carbonyl)-

Supply Marketing:

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

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Chemical Property of Benzamide, 2,6-difluoro-N-((phenylamino)carbonyl)-

Chemical Property:

Boiling Point:°Cat760mmHg
Flash Point:°C
Density:1.386g/cm³
XLogP3:3.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:276.07103389
Heavy Atom Count:20
Complexity:349

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C=C1)NC(=O)NC(=O)C2=C(C=CC=C2F)F

Technology Process of Benzamide, 2,6-difluoro-N-((phenylamino)carbonyl)-

There total 4 articles about Benzamide, 2,6-difluoro-N-((phenylamino)carbonyl)- 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: 74.0%

: 64-10-8
phenyl carbamate

: 172505-58-7
2,6-Difluoro-benzoic acid 1-methylene-pentyl ester

: 57160-53-9
1-(2,6-Difluoro-benzoyl)-3-phenyl-urea

Guidance literature:: With sodium hydride; In tetrahydrofuran; for 2h; Ambient temperature;
DOI:10.1016/0040-4020(95)00666-V

Reference yield: 73.0%

: 60731-73-9
2,6-difluorobenzoyl isocyanate

: 62-53-3
aniline

: 57160-53-9
1-(2,6-Difluoro-benzoyl)-3-phenyl-urea

Guidance literature:: In benzene; for 0.5h; Ambient temperature;
DOI:10.1016/S0040-4020(01)89797-0

Reference yield:

: 18063-02-0
2,6-difluorobenzoylchloride

: 57160-53-9
1-(2,6-Difluoro-benzoyl)-3-phenyl-urea

Guidance literature:: Multi-step reaction with 2 steps

1: 70 percent / SnCl₄ / 1,2-dichloro-benzene / 2 h / Heating

2: 73 percent / benzene / 0.5 h / Ambient temperature

tin(IV) chloride; In 1,2-dichloro-benzene; benzene;
DOI:10.1016/S0040-4020(01)89797-0