2-chloro-N-ethylbenzamide

Base Information

Chemical Name:2-chloro-N-ethylbenzamide
CAS No.:66896-65-9
Molecular Formula:C9H10ClNO
Molecular Weight:183.637
Hs Code.:
NSC Number:406907
DSSTox Substance ID:DTXSID80324519
Nikkaji Number:J419.215J
Wikidata:Q82084218

Synonyms:2-chloro-N-ethylbenzamide;66896-65-9;NSC406907;N-Ethyl-2-Chlorobenzamide;Benzamide, 2-chloro-N-ethyl-;SCHEMBL4148749;DTXSID80324519;MFCD01211890;STL071220;AKOS000499868;NSC 406907;NSC-406907;AN-329/11633891;Z32024315

Suppliers and Price of 2-chloro-N-ethylbenzamide

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

Aronis compounds
2-chloro-N-ethylbenzamide
50mg
$ 50.00

American Custom Chemicals Corporation
2-CHLORO-N-ETHYLBENZAMIDE 95.00%
5MG
$ 502.71

Total 6 raw suppliers

Chemical Property of 2-chloro-N-ethylbenzamide

Chemical Property:

Vapor Pressure:0.000615mmHg at 25°C
Boiling Point:310°Cat760mmHg
Flash Point:141.3°C
PSA：29.10000
Density:1.16g/cm³
LogP:2.48060
XLogP3:1.3
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:2
Exact Mass:183.0450916
Heavy Atom Count:12
Complexity:161

Purity/Quality:

99.5% ^*data from raw suppliers

2-chloro-N-ethylbenzamide ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCNC(=O)C1=CC=CC=C1Cl

Technology Process of 2-chloro-N-ethylbenzamide

There total 3 articles about 2-chloro-N-ethylbenzamide 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:

: 609-65-4
o-chlorobenzoyl chloride

: 75-04-7,85404-22-4
ethylamine

: 66896-65-9
2-chloro-N-ethyl-benzamide

Guidance literature:

Reference yield:

: 118-91-2
ortho-chlorobenzoic acid

: 66896-65-9
2-chloro-N-ethyl-benzamide

Guidance literature:: Multi-step reaction with 2 steps

1: thionyl chloride / 2 h / Reflux

2: potassium carbonate / tetrahydrofuran / Cooling with ice

With thionyl chloride; potassium carbonate; In tetrahydrofuran;
DOI:10.1039/c1cc15843k