N-(2-acetylaminoethyl)-4-chlorobenzamide

Base Information

Chemical Name:N-(2-acetylaminoethyl)-4-chlorobenzamide
CAS No.:94320-01-1
Molecular Formula:C11H13ClN2O2
Molecular Weight:240.689
Hs Code.:
DSSTox Substance ID:DTXSID301268159

Synonyms:N-(2-acetylaminoethyl)-4-chlorobenzamide;94320-01-1;SCHEMBL8202479;HRKSQNAYPHEBQO-UHFFFAOYSA-N;DTXSID301268159;AKOS027674715;N-[2-(Acetylamino)ethyl]-4-chlorobenzamide;Z32152910

Suppliers and Price of N-(2-acetylaminoethyl)-4-chlorobenzamide

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 N-(2-acetylaminoethyl)-4-chlorobenzamide

Chemical Property:

XLogP3:1.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:240.0665554
Heavy Atom Count:16
Complexity:250

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CC(=O)NCCNC(=O)C1=CC=C(C=C1)Cl

Technology Process of N-(2-acetylaminoethyl)-4-chlorobenzamide

There total 3 articles about N-(2-acetylaminoethyl)-4-chlorobenzamide 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:

: 1001-53-2
monoacetylaminoethylamine

: 122-01-0
4-chloro-benzoyl chloride

: 94320-01-1
N-(2-acetylaminoethyl)-4-chlorobenzamide

Guidance literature:: With triethylamine; In chloroform; for 2h; Ambient temperature;
DOI:10.1248/cpb.40.1789

Reference yield:

: 74-11-3
para-chlorobenzoic acid

: 94320-01-1
N-(2-acetylaminoethyl)-4-chlorobenzamide

Guidance literature:: Multi-step reaction with 2 steps

1: SOCl₂ / 2 h / Heating

2: Et₃N / CHCl₃ / 2 h / Ambient temperature

With thionyl chloride; triethylamine; In chloroform;
DOI:10.1248/cpb.40.1789