2-(2-chlorophenyl)-N-hydroxyacetamide

Base Information

Chemical Name:2-(2-chlorophenyl)-N-hydroxyacetamide
CAS No.:2593-89-7
Molecular Formula:C₈H₈ClNO₂
Molecular Weight:185.61
Hs Code.:
DSSTox Substance ID:DTXSID501297774
Nikkaji Number:J1.389.014E
ChEMBL ID:CHEMBL2359526

Synonyms:2-(2-chlorophenyl)-N-hydroxyacetamide;2593-89-7;CHEMBL2359526;2-Chloro-N-hydroxybenzeneacetamide;2-Chlorobenzeneacetohydroxamic acid;DTXSID501297774;CAA59389;AKOS000185539;NCGC00186608-01;CS-0251079;EN300-53493;Z59182782

Suppliers and Price of 2-(2-chlorophenyl)-N-hydroxyacetamide

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 2-(2-chlorophenyl)-N-hydroxyacetamide

Chemical Property:

XLogP3:1.3
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:2
Exact Mass:185.0243562
Heavy Atom Count:12
Complexity:163

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC=C(C(=C1)CC(=O)NO)Cl

Technology Process of 2-(2-chlorophenyl)-N-hydroxyacetamide

There total 3 articles about 2-(2-chlorophenyl)-N-hydroxyacetamide 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:

: C₁₁H₁₁ClO₄

: 2593-89-7
<2-Chlor-phenyl>-acethydroxamsaeure

Guidance literature:: With hydroxylamine; In methanol; diethyl ether; at 20 ℃; for 0.5h;
DOI:10.1016/S0040-4039(00)01058-3

Reference yield:

: 2444-36-2
2'-chloro-benzeneacetic acid

: 2593-89-7
<2-Chlor-phenyl>-acethydroxamsaeure

Guidance literature:: Multi-step reaction with 2 steps

1: N-methylmorpholine / diethyl ether / 0.17 h / 0 °C

2: hydroxylamine / diethyl ether; methanol / 0.5 h / 20 °C

With 4-methyl-morpholine; hydroxylamine; In methanol; diethyl ether; 1: Condensation / 2: amidation;
DOI:10.1016/S0040-4039(00)01058-3