2-(Chloroacetylamino)-6-methylbenzoic acid

Base Information

Chemical Name:2-(Chloroacetylamino)-6-methylbenzoic acid
CAS No.:66232-40-4
Molecular Formula:C10H10ClNO3
Molecular Weight:227.647
Hs Code.:
DSSTox Substance ID:DTXSID201245786
Nikkaji Number:J3.124.012C

Synonyms:SCHEMBL474148;HPAYNZVLUHWQSV-UHFFFAOYSA-N;DTXSID201245786;66232-40-4;2-(Chloroacetylamino)-6-methylbenzoic acid;2-(-2-chloroacetamido)-6-methylbenzoic acid;2-[(2-chloroacetyl)amino]-6-methylbenzoic acid

Suppliers and Price of 2-(Chloroacetylamino)-6-methylbenzoic acid

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 0 raw suppliers

Chemical Property of 2-(Chloroacetylamino)-6-methylbenzoic acid

Chemical Property:

XLogP3:2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:3
Exact Mass:227.0349209
Heavy Atom Count:15
Complexity:257

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC1=C(C(=CC=C1)NC(=O)CCl)C(=O)O

Technology Process of 2-(Chloroacetylamino)-6-methylbenzoic acid

There total 2 articles about 2-(Chloroacetylamino)-6-methylbenzoic acid 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: 100.0%

: 4389-50-8
2-amino-6-methylbenzoic acid

: 79-04-9
chloroacetyl chloride

: 66232-40-4
2-[(chloroacetyl)amino]-6-methylbenzoic acid

Guidance literature:: With triethylamine; In tetrahydrofuran; at 0 - 20 ℃; Inert atmosphere;
DOI:10.1016/j.tetlet.2012.08.137 DOI:10.1016/j.tetlet.2012.08.137