5-Phenylpent-1-en-3-one

Base Information

Chemical Name:5-Phenylpent-1-en-3-one
CAS No.:53931-59-2
Molecular Formula:C11H12O
Molecular Weight:160.216
Hs Code.:
DSSTox Substance ID:DTXSID80393503
Nikkaji Number:J698.859H
Wikidata:Q82192293
Mol file:53931-59-2.mol

Synonyms:5-phenylpent-1-en-3-one;53931-59-2;5-Phenyl-1-penten-3-one;SCHEMBL4424144;DTXSID80393503;AKOS014915467;EN300-1869952

Suppliers and Price of 5-Phenylpent-1-en-3-one

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 5-Phenylpent-1-en-3-one

Chemical Property:

XLogP3:2.4
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:1
Rotatable Bond Count:4
Exact Mass:160.088815002
Heavy Atom Count:12
Complexity:154

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C=CC(=O)CCC1=CC=CC=C1

Technology Process of 5-Phenylpent-1-en-3-one

There total 21 articles about 5-Phenylpent-1-en-3-one 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: 100.0%

: 37904-38-4
5-phenylpent-1-en-3-ol

: 53931-59-2
5-phenyl-1-penten-3-one

Guidance literature:: With 1-hydroxy-3H-benz[d][1,2]iodoxole-1,3-dione; In tetrahydrofuran; dimethyl sulfoxide; at 20 ℃; for 2h;
DOI:10.1021/jo802453m

Reference yield: 93.0%

: 16900-77-9
5-phenyl-2-pentynol

: 53931-59-2
5-phenyl-1-penten-3-one

Guidance literature:: With bis(acetylacetonato)dioxidomolybdenum(VI); triphenylphosphine gold (I) chloride; silver trifluoromethanesulfonate; In toluene; at 20 ℃; for 0.5h;
DOI:10.1021/ol800596c