Benzeneacetamide, alpha-oxo-N-(1-phenylpropyl)-, (S)-

Base Information

Chemical Name:Benzeneacetamide, alpha-oxo-N-(1-phenylpropyl)-, (S)-
CAS No.:10549-18-5
Molecular Formula:C17H17NO2
Molecular Weight:267.327
Hs Code.:
DSSTox Substance ID:DTXSID201230797

Synonyms:Benzeneacetamide, alpha-oxo-N-(1-phenylpropyl)-, (S)-;DTXSID201230797;10549-18-5

Suppliers and Price of Benzeneacetamide, alpha-oxo-N-(1-phenylpropyl)-, (S)-

Supply Marketing:

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

Manufacturers and distributors:

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Total 0 raw suppliers

Chemical Property of Benzeneacetamide, alpha-oxo-N-(1-phenylpropyl)-, (S)-

Chemical Property:

XLogP3:3.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:5
Exact Mass:267.125928785
Heavy Atom Count:20
Complexity:328

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCC(C1=CC=CC=C1)NC(=O)C(=O)C2=CC=CC=C2
Isomeric SMILES:CC[C@@H](C1=CC=CC=C1)NC(=O)C(=O)C2=CC=CC=C2

Technology Process of Benzeneacetamide, alpha-oxo-N-(1-phenylpropyl)-, (S)-

There total 2 articles about Benzeneacetamide, alpha-oxo-N-(1-phenylpropyl)-, (S)- 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: 55.0%

: 25726-04-9
phenylglyoxylyl chloride

: 3789-59-1
(R)-1-phenylpropylamine

: 10549-18-5
N-<(S)-α-ethylbenzyl>benzoylformamide

Guidance literature:: With triethylamine; In benzene; 5-10 deg C, 2 h; room temperature, 12 h;
DOI:10.1246/bcsj.57.3203

Reference yield:

: 611-73-4
Benzoylformic acid

: 10549-18-5
N-<(S)-α-ethylbenzyl>benzoylformamide

Guidance literature:: Multi-step reaction with 2 steps

1: 56 percent / (COCl)2 / 6 h / Heating

2: 55 percent / (C₂H₅)3N / benzene / 5-10 deg C, 2 h; room temperature, 12 h

With oxalyl dichloride; triethylamine; In benzene;
DOI:10.1246/bcsj.57.3203

Reference yield:

: 10549-18-5
N-<(S)-α-ethylbenzyl>benzoylformamide

: (R)-2-Hydroxy-2-phenyl-N-((S)-1-phenyl-propyl)-acetamide

: (S)-2-Hydroxy-2-phenyl-N-((S)-1-phenyl-propyl)-acetamide

Guidance literature:: With hydrogen; palladium on activated charcoal; In methanol; at 30 ℃; for 9h; Product distribution; var. solvents, oth. temperature;
DOI:10.1246/bcsj.57.3203