Acetamide, N-(2-oxopropyl)-N-(phenylmethyl)-

Base Information

Chemical Name:Acetamide, N-(2-oxopropyl)-N-(phenylmethyl)-
CAS No.:61357-16-2
Molecular Formula:C12H15NO2
Molecular Weight:205.257
Hs Code.:
DSSTox Substance ID:DTXSID30461600
Nikkaji Number:J2.045.208K
Wikidata:Q82285971

Synonyms:61357-16-2;Acetamide, N-(2-oxopropyl)-N-(phenylmethyl)-;DTXSID30461600

Suppliers and Price of Acetamide, N-(2-oxopropyl)-N-(phenylmethyl)-

Supply Marketing:

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

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Chemical Property of Acetamide, N-(2-oxopropyl)-N-(phenylmethyl)-

Chemical Property:

XLogP3:1
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:205.110278721
Heavy Atom Count:15
Complexity:232

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

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

Technology Process of Acetamide, N-(2-oxopropyl)-N-(phenylmethyl)-

There total 2 articles about Acetamide, N-(2-oxopropyl)-N-(phenylmethyl)- 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: 75.0%

: 64-19-7,77671-22-8
acetic acid

: 188818-06-6
N-benzyl-2-methylene-aziridine

: 61357-16-2
N-benzyl-N-(2-oxo-propyl)-acetamide

Guidance literature:: With tris(dibenzylideneacetone)dipalladium⁽⁰⁾ chloroform complex; triphenylphosphine; In tetrahydrofuran; at 100 ℃;
DOI:10.1021/jo035739g

Reference yield:

: 6436-91-5
ethyl N-acetyl-N-benzylaminoacetate

: 16812-43-4
bis(trimethylstannyl)methane

: 113133-50-9
N-benzyl-N-(2-methylallyl)acetamide

: 61357-16-2
N-benzyl-N-(2-oxo-propyl)-acetamide

Guidance literature:: With n-butyllithium; Yield given. Multistep reaction. Yields of byproduct given; 1.) THF, hexane, -78 deg C, 10 min, 2.) -78 deg C, 5 h;
DOI:10.1021/jo00241a016