3-Chloro-N-[3-(1H-imidazol-1-yl)propyl]benzeneacetamide

Base Information

Chemical Name:3-Chloro-N-[3-(1H-imidazol-1-yl)propyl]benzeneacetamide
CAS No.:93668-69-0
Molecular Formula:C₁₄H₁₆ClN₃O
Molecular Weight:277.754
Hs Code.:
ChEMBL ID:CHEMBL359004
DSSTox Substance ID:DTXSID001204045

Synonyms:CHEMBL359004;SCHEMBL10856361;3-Chloro-N-[3-(1H-imidazol-1-yl)propyl]benzeneacetamide;DTXSID001204045;93668-69-0

Suppliers and Price of 3-Chloro-N-[3-(1H-imidazol-1-yl)propyl]benzeneacetamide

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 3 raw suppliers

Chemical Property of 3-Chloro-N-[3-(1H-imidazol-1-yl)propyl]benzeneacetamide

Chemical Property:

XLogP3:1.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:6
Exact Mass:277.0981898
Heavy Atom Count:19
Complexity:288

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1=CC(=CC(=C1)Cl)CC(=O)NCCCN2C=CN=C2

Technology Process of 3-Chloro-N-[3-(1H-imidazol-1-yl)propyl]benzeneacetamide

There total 2 articles about 3-Chloro-N-[3-(1H-imidazol-1-yl)propyl]benzeneacetamide 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:

: 1878-65-5
3-chlorophenylacetic acid

: 93668-69-0
3-Chloro-N-[3-(1H-Imidazol-1-yl)propyl]benzeneacetamide

Guidance literature:

Reference yield:

: 1878-65-5
3-chlorophenylacetic acid

: 17583-33-4,100468-35-7
3-imidazol-1-yl-propylamine; dihydrochloride

: 93668-69-0
3-Chloro-N-[3-(1H-Imidazol-1-yl)propyl]benzeneacetamide

Guidance literature:: With 1,1'-carbonyldiimidazole; Multistep reaction; 1.) THF, RT, 2 h, 2.) THF, from RT to reflux;
DOI:10.1021/jm00154a017