Benzoic acid, 2-((aminocarbonyl)oxy)-, 4-chlorophenyl ester

Base Information

Chemical Name:Benzoic acid, 2-((aminocarbonyl)oxy)-, 4-chlorophenyl ester
CAS No.:88599-62-6
Molecular Formula:C14H10ClNO4
Molecular Weight:291.691
Hs Code.:
DSSTox Substance ID:DTXSID70237184
Wikidata:Q83119282

Synonyms:BRN 5073693;4-Chlorophenyl 2-((aminocarbonyl)oxy)benzoate;Benzoic acid, 2-((aminocarbonyl)oxy)-, 4-chlorophenyl ester;88599-62-6;DTXSID70237184;LS-35678

Suppliers and Price of Benzoic acid, 2-((aminocarbonyl)oxy)-, 4-chlorophenyl ester

Supply Marketing:

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

Manufacturers and distributors:

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Chemical Property of Benzoic acid, 2-((aminocarbonyl)oxy)-, 4-chlorophenyl ester

Chemical Property:

Vapor Pressure:8.28E-10mmHg at 25°C
Boiling Point:491.6°Cat760mmHg
Flash Point:251.1°C
Density:1.391g/cm³
XLogP3:2.9
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:5
Exact Mass:291.0298355
Heavy Atom Count:20
Complexity:355

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC=C(C(=C1)C(=O)OC2=CC=C(C=C2)Cl)OC(=O)N

Technology Process of Benzoic acid, 2-((aminocarbonyl)oxy)-, 4-chlorophenyl ester

There total 1 articles about Benzoic acid, 2-((aminocarbonyl)oxy)-, 4-chlorophenyl ester 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:

: 1189-71-5
isocyanate de chlorosulfonyle

: 2944-58-3
4-chlorophenyl 2-hydroxybenzoate

: 88599-62-6
2-Carbamoyloxy-benzoic acid 4-chloro-phenyl ester

Guidance literature:: With water; Yield given. Multistep reaction; 1.) dichloromethane, 4-6 deg C, 20 min; 2.) 5-10 deg C, 36 h;
DOI:10.1016/0223-5234(88)90148-1

Reference yield:

: 88599-62-6
2-Carbamoyloxy-benzoic acid 4-chloro-phenyl ester

: 2037-95-8
1,3-benzoxazine-2,4-dione

: 65-45-2
salicylamide

Guidance literature:: In ethanol; water; at 35 - 37 ℃; for 18h; Title compound not separated from byproducts; rat liver microsomes, pH 7.4;
DOI:10.1021/jo00252a045