(E)-1-(4-methoxyphenyl)non-1-en-3-one

Base Information

Chemical Name:(E)-1-(4-methoxyphenyl)non-1-en-3-one
CAS No.:74975-53-4
Molecular Formula:C16H22 O2
Molecular Weight:246.349
Hs Code.:
NSC Number:311447
DSSTox Substance ID:DTXSID50422990
Wikidata:Q82235086

Synonyms:NSC311447;74975-53-4;DTXSID50422990;NSC-311447

Suppliers and Price of (E)-1-(4-methoxyphenyl)non-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 5 raw suppliers

Chemical Property of (E)-1-(4-methoxyphenyl)non-1-en-3-one

Chemical Property:

Vapor Pressure:3.17E-06mmHg at 25°C
Boiling Point:388°Cat760mmHg
Flash Point:164.1°C
Density:0.983g/cm³
XLogP3:4.5
Hydrogen Bond Donor Count:0
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:8
Exact Mass:246.161979940
Heavy Atom Count:18
Complexity:250

Purity/Quality:: 99% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CCCCCCC(=O)C=CC1=CC=C(C=C1)OC
Isomeric SMILES:CCCCCCC(=O)/C=C/C1=CC=C(C=C1)OC

Technology Process of (E)-1-(4-methoxyphenyl)non-1-en-3-one

There total 1 articles about (E)-1-(4-methoxyphenyl)non-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: 60.0%

: 123-11-5
4-methoxy-benzaldehyde

: 111-13-7
hexyl-methyl-ketone

: 74975-53-4
(E)-1-(4-methoxyphenyl)non-1-en-3-one

Guidance literature:: With cycl-isopropylidene malonate; N,N-dimethylethylenediamine; In ethyl acetate; at 55 ℃; for 24h; diastereoselective reaction;
DOI:10.1016/j.tetlet.2018.11.065