N-[(S)-1-Benzylpropyl]acetamide

Base Information

Chemical Name:N-[(S)-1-Benzylpropyl]acetamide
CAS No.:69622-20-4
Molecular Formula:C₁₂H₁₇NO
Molecular Weight:191.273
Hs Code.:
DSSTox Substance ID:DTXSID501275926
Nikkaji Number:J1.654.087K

Synonyms:SCHEMBL17305286;DTXSID501275926;N-[(S)-1-Benzylpropyl]acetamide;N-[(1S)-1-(Phenylmethyl)propyl]acetamide;69622-20-4

Suppliers and Price of N-[(S)-1-Benzylpropyl]acetamide

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-[(S)-1-Benzylpropyl]acetamide

Chemical Property:

XLogP3:2.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:191.131014166
Heavy Atom Count:14
Complexity:173

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:CCC(CC1=CC=CC=C1)NC(=O)C
Isomeric SMILES:CC[C@@H](CC1=CC=CC=C1)NC(=O)C

Technology Process of N-[(S)-1-Benzylpropyl]acetamide

There total 8 articles about N-[(S)-1-Benzylpropyl]acetamide 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:

: 222016-68-4
(R,R)-p-Chlorophenyl-1-chloro-2-phenylethyl sulfoxide

: 69622-20-4
(N)-(1-phenyl-2-butyl)acetamide

Guidance literature:: Multi-step reaction with 3 steps

1.1: tetrahydrofuran / -78 - -30 °C

1.2: anhydrous zinc(II) chloride / tetrahydrofuran / 1.33 h / -78 °C

1.3: copper(II) chloride / tetrahydrofuran / -78 - 20 °C

2.1: hydrogen / palladium on carbon / ethanol / 2 h / 11400.8 Torr

3.1: triethylamine / CH₂Cl₂ / 1 h / 20 °C

With hydrogen; triethylamine; palladium on activated charcoal; In tetrahydrofuran; ethanol; dichloromethane;
DOI:10.1021/ol0702829

Reference yield:

: 108-24-7
acetic anhydride

: 30543-90-9
(S)-1-Benzyl-propylamine

: 69622-20-4
(N)-(1-phenyl-2-butyl)acetamide

Guidance literature:: With triethylamine; In dichloromethane; at 20 ℃; for 1h;
DOI:10.1021/ol0702829

Reference yield:

: C₂₄H₂₇N

: 69622-20-4
(N)-(1-phenyl-2-butyl)acetamide

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogen / palladium on carbon / ethanol / 2 h / 11400.8 Torr

2: triethylamine / CH₂Cl₂ / 1 h / 20 °C

With hydrogen; triethylamine; palladium on activated charcoal; In ethanol; dichloromethane;
DOI:10.1021/ol0702829