N-benzyl-4-chloro-N-methylbutanamide

Base Information

Chemical Name:N-benzyl-4-chloro-N-methylbutanamide
CAS No.:671220-23-8
Molecular Formula:C12H16ClNO
Molecular Weight:225.718
Hs Code.:
DSSTox Substance ID:DTXSID80602748
Wikidata:Q82499917

Synonyms:N-benzyl-4-chloro-N-methylbutanamide;671220-23-8;SCHEMBL415549;DTXSID80602748;AKOS000158139

Suppliers and Price of N-benzyl-4-chloro-N-methylbutanamide

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 1 raw suppliers

Chemical Property of N-benzyl-4-chloro-N-methylbutanamide

Chemical Property:

XLogP3:2.1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:5
Exact Mass:225.0920418
Heavy Atom Count:15
Complexity:190

Purity/Quality:: 85.0-99.8% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CN(CC1=CC=CC=C1)C(=O)CCCCl

Technology Process of N-benzyl-4-chloro-N-methylbutanamide

There total 3 articles about N-benzyl-4-chloro-N-methylbutanamide 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: 91.0%

: 202402-02-6
N-benzyl-4-hydroxy-N-methylbutyramide

: 671220-23-8
N-benzyl-4-chloro-N-methylbutyramide

Guidance literature:: With thionyl chloride; In chloroform; at 20 ℃; for 2h;
DOI:10.1016/S0014-827X(03)00111-3

Reference yield: 80.0%

: 103-67-3
benzyl-methyl-amine

: 4635-59-0
4-Chlorobutanoyl chloride

: 671220-23-8
N-benzyl-4-chloro-N-methylbutyramide

Guidance literature:: In diethyl ether; at 20 ℃; for 1h;
DOI:10.1016/j.tet.2004.03.073

Reference yield:

: 103-67-3
benzyl-methyl-amine

: 671220-23-8
N-benzyl-4-chloro-N-methylbutyramide

Guidance literature:: Multi-step reaction with 2 steps

1: 89 percent / 20 h / 70 °C

2: 91 percent / SOCl₂ / CHCl₃ / 2 h / 20 °C

With thionyl chloride; In chloroform;
DOI:10.1016/S0014-827X(03)00111-3