2-Pyrrolidinone, 5-methylene-1-phenyl-

Base Information

Chemical Name:2-Pyrrolidinone, 5-methylene-1-phenyl-
CAS No.:96326-28-2
Molecular Formula:C11H11NO
Molecular Weight:173.214
Hs Code.:
DSSTox Substance ID:DTXSID30472635
Nikkaji Number:J2.179.488K
Wikidata:Q82301647

Synonyms:2-Pyrrolidinone, 5-methylene-1-phenyl-;96326-28-2;SCHEMBL15834910;DTXSID30472635

Suppliers and Price of 2-Pyrrolidinone, 5-methylene-1-phenyl-

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 2-Pyrrolidinone, 5-methylene-1-phenyl-

Chemical Property:

XLogP3:1.7
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:1
Exact Mass:173.084063974
Heavy Atom Count:13
Complexity:228

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=C1CCC(=O)N1C2=CC=CC=C2

Technology Process of 2-Pyrrolidinone, 5-methylene-1-phenyl-

There total 3 articles about 2-Pyrrolidinone, 5-methylene-1-phenyl- 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%

: 4-iodo-N-phenylpent-4-enamide

: 96326-28-2
5-Methylene-1-phenyl-pyrrolidin-2-one

Guidance literature:: With copper(l) iodide; caesium carbonate; N,N`-dimethylethylenediamine; In 1,4-dioxane; for 20h; Heating;
DOI:10.1021/ol0505555

Reference yield:

: 62-53-3
aniline

: 96326-28-2
5-Methylene-1-phenyl-pyrrolidin-2-one

Guidance literature:: Multi-step reaction with 2 steps

1: polyphosphoric acid / 12 h / 80 °C

2: tetrahydrofuran / 65 °C

With polyphosphoric acid; In tetrahydrofuran;
DOI:10.1016/j.tetlet.2014.03.021