Intricatinol

Base Information

Chemical Name:Intricatinol
CAS No.:124166-26-3
Molecular Formula:C17H14 O5
Molecular Weight:298.29006
Hs Code.:
Nikkaji Number:J494.242F
Metabolomics Workbench ID:128354
ChEMBL ID:CHEMBL233805
Mol file:124166-26-3.mol

Synonyms:4'-methoxy-7,8-dihydroxyhomoisoflavone;intricatinol

Suppliers and Price of Intricatinol

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 3 raw suppliers

Chemical Property of Intricatinol

Chemical Property:

Vapor Pressure:4.51E-14mmHg at 25°C
Boiling Point:580.4°Cat760mmHg
Flash Point:219.7°C
PSA：75.99000
Density:1.404g/cm³
LogP:2.76510
XLogP3:2.6
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:2
Exact Mass:298.08412354
Heavy Atom Count:22
Complexity:438

Purity/Quality:: 98%min ^*data from raw suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC=C(C=C1)C=C2COC3=C(C2=O)C=CC(=C3O)O
Isomeric SMILES:COC1=CC=C(C=C1)/C=C/2\COC3=C(C2=O)C=CC(=C3O)O

Technology Process of Intricatinol

There total 3 articles about Intricatinol 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

: 59887-99-9
7,8-dihydroxy-4-oxo-4H-1-benzopyran

: 124166-26-3
(E)-7,8-dihydroxy-3-(4-methoxybenzylidene)chroman-4-one

Guidance literature:: With piperidine; at 70 - 80 ℃; for 2h;
DOI:10.1016/j.bmcl.2006.12.008

Reference yield:

: 19149-07-6
7,8-dimethoxy-2,3-dihydrochromen-4-one

: 124166-26-3
(E)-7,8-dihydroxy-3-(4-methoxybenzylidene)chroman-4-one

Guidance literature:: Multi-step reaction with 2 steps

1: aqueous hydrobromic acid

2: ethanol; hydrogen chloride

With hydrogenchloride; ethanol; hydrogen bromide;