3-Chloro-N-(4-cyclopentylphenyl)propanamide

Base Information

Chemical Name:3-Chloro-N-(4-cyclopentylphenyl)propanamide
CAS No.:85603-07-2
Molecular Formula:C14H18ClNO
Molecular Weight:251.756
Hs Code.:
DSSTox Substance ID:DTXSID10574762
Wikidata:Q82463920

Synonyms:3-Chloro-N-(4-cyclopentylphenyl)propanamide;85603-07-2;DTXSID10574762

Suppliers and Price of 3-Chloro-N-(4-cyclopentylphenyl)propanamide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

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Chemical Property of 3-Chloro-N-(4-cyclopentylphenyl)propanamide

Chemical Property:

XLogP3:3.8
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:251.1076919
Heavy Atom Count:17
Complexity:243

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1CCC(C1)C2=CC=C(C=C2)NC(=O)CCCl

Technology Process of 3-Chloro-N-(4-cyclopentylphenyl)propanamide

There total 3 articles about 3-Chloro-N-(4-cyclopentylphenyl)propanamide 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: 95.0%

: 20029-53-2
(4-aminophenyl)cyclopentane

: 625-36-5
2-chloropropionyl chloride

: 85603-07-2
N-(4-cyclopentylphenyl)-3-chloropropionamide

Guidance literature:: With potassium carbonate; In chloroform; for 1.5h; Heating;
DOI:10.1135/cccc19830156

Reference yield:

: 80649-39-4
4-Cyclopentylacetophenone Oxime

: 85603-07-2
N-(4-cyclopentylphenyl)-3-chloropropionamide

Guidance literature:: Multi-step reaction with 2 steps

1: 1) PCl₅; 2) aq. HCl / 1) Et₂O; 2) EtOH, reflux, 3 h

2: 95 percent / K₂CO₃ / CHCl₃ / 1.5 h / Heating

With hydrogenchloride; phosphorus pentachloride; potassium carbonate; In chloroform;
DOI:10.1135/cccc19830156

Reference yield:

: 85602-98-8
N-(4-Cyclopentylphenyl)acetamide

: 85603-07-2
N-(4-cyclopentylphenyl)-3-chloropropionamide

Guidance literature:: Multi-step reaction with 2 steps

1: 75 percent / aq. HCl / ethanol / 3 h / Heating

2: 95 percent / K₂CO₃ / CHCl₃ / 1.5 h / Heating

With hydrogenchloride; potassium carbonate; In ethanol; chloroform;
DOI:10.1135/cccc19830156