Benzoic acid, 2-[(chloroacetyl)phenylamino]-, methyl ester

Base Information

Chemical Name:Benzoic acid, 2-[(chloroacetyl)phenylamino]-, methyl ester
CAS No.:91855-59-3
Molecular Formula:C16H14ClNO3
Molecular Weight:303.745
Hs Code.:
DSSTox Substance ID:DTXSID10524489
Wikidata:Q82391385

Synonyms:91855-59-3;Benzoic acid, 2-[(chloroacetyl)phenylamino]-, methyl ester;Methyl 2-[(chloroacetyl)(phenyl)amino]benzoate;DTXSID10524489

Suppliers and Price of Benzoic acid, 2-[(chloroacetyl)phenylamino]-, methyl ester

Supply Marketing:

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

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Chemical Property of Benzoic acid, 2-[(chloroacetyl)phenylamino]-, methyl ester

Chemical Property:

XLogP3:3.3
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:5
Exact Mass:303.0662210
Heavy Atom Count:21
Complexity:369

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC(=O)C1=CC=CC=C1N(C2=CC=CC=C2)C(=O)CCl

Technology Process of Benzoic acid, 2-[(chloroacetyl)phenylamino]-, methyl ester

There total 3 articles about Benzoic acid, 2-[(chloroacetyl)phenylamino]-, methyl 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: 66.0%

: 35708-19-1
Methyl N-phenylanthranilate

: 79-04-9
chloroacetyl chloride

: 91855-59-3
N-Chloracetyl-N-phenylanthranilsaeuremethylester

Guidance literature:: In benzene; for 48h; Ambient temperature;
DOI:10.1002/ardp.19843170705

Reference yield:

: 91-40-7
2-(phenylamino)benzoic acid

: 91855-59-3
N-Chloracetyl-N-phenylanthranilsaeuremethylester

Guidance literature:: Multi-step reaction with 2 steps

1: 81 percent / conc. H₂SO₄ / 12 h / Heating

2: 66 percent / benzene / 48 h / Ambient temperature

With sulfuric acid; In benzene;
DOI:10.1002/ardp.19843170705