Turmeronol A

Base Information

Chemical Name:Turmeronol A
CAS No.:131651-37-1
Molecular Formula:C15H20 O2
Molecular Weight:232.32
Hs Code.:
DSSTox Substance ID:DTXSID001317951
Nikkaji Number:J367.156I
Wikidata:Q105198921
Mol file:131651-37-1.mol

Synonyms:2-Hepten-4-one, 6-(3-hydroxy-4-methylphenyl)-2-methyl-;6-(3-Hydroxy-4-methylphenyl)-2-methyl-2-hepten-4-one;turmeronol A

Suppliers and Price of Turmeronol A

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 Turmeronol A

Chemical Property:

PSA：37.30000
LogP:3.72950
XLogP3:3.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:4
Exact Mass:232.146329876
Heavy Atom Count:17
Complexity:289

Purity/Quality:: 98.0% ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC1=C(C=C(C=C1)C(C)CC(=O)C=C(C)C)O
Isomeric SMILES:CC1=C(C=C(C=C1)[C@@H](C)CC(=O)C=C(C)C)O

Technology Process of Turmeronol A

There total 24 articles about Turmeronol A 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: 99.0%

: 38614-36-7
2-methylpropen-1-ylmagnesium bromide

: 246037-78-5
3-(3-hydroxy-4-methyl-phenyl)-N-methoxy-N-methyl-butyramide

: 131651-37-1
(S)-turmeronol A

Guidance literature:: In tetrahydrofuran;
DOI:10.1248/cpb.47.1053

Reference yield: 93.0%

: formyl-ar-turmerone

: 131651-37-1
(S)-turmeronol A

Guidance literature:: formyl-ar-turmerone; With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; for 1h;

With sodium hydrogencarbonate; In methanol; dichloromethane; water; at 20 ℃; for 1h;
DOI:10.1021/acs.joc.9b01298