(+)-Isoxanthochymol

Base Information

Chemical Name:(+)-Isoxanthochymol
CAS No.:52617-33-1
Molecular Formula:C₃₈H₅₀O₆
Molecular Weight:602.811
Hs Code.:
Metabolomics Workbench ID:122245

Synonyms:isoxanthochymol

Suppliers and Price of (+)-Isoxanthochymol

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 33 raw suppliers

Chemical Property of (+)-Isoxanthochymol

Chemical Property:

Vapor Pressure:7.7E-21mmHg at 25°C
Boiling Point:710.2°Cat760mmHg
Flash Point:213.4°C
PSA：100.90000
Density:1.16g/cm³
LogP:8.58930
XLogP3:8.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:8
Exact Mass:602.36073931
Heavy Atom Count:44
Complexity:1310

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

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=CCC1CC23CC(C(OC2=C(C(=O)C(C3=O)(C1(C)C)CC=C(C)C)C(=O)C4=CC(=C(C=C4)O)O)(C)C)CC=C(C)C)C
General Description **Conclusion:** 10-(3,4-Dihydroxybenzoyl)-3,4,5,6,7,8-hexahydro-2,2,7,7-tetramethyl-3α,6α,8-tris(3-methyl-2-butenyl)-9H-4aβ,8β-methano-2H-cycloocta[b]pyran-9,11-dione is a polyisoprenylated benzophenone derivative structurally related to compounds like garcinol, isogarcinol, and the guttiferones. These compounds exhibit notable biological activity, including HIV-inhibitory effects, and are characterized by their complex polycyclic frameworks and isoprenyl side chains. The structural elucidation of such derivatives has been resolved through methods like X-ray crystallography and spectral analysis.

Technology Process of (+)-Isoxanthochymol

There total 12 articles about (+)-Isoxanthochymol 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:

: 147782-04-5
Guttiferone E

: 52617-33-1,71117-97-0
(+)-isoxanthochymol

Guidance literature:: With hydrogenchloride; In toluene; for 0.5h; Heating;
DOI:10.1016/S0040-4020(01)89039-6

Reference yield:

: (+)-xanthochymol

: 52617-33-1,71117-97-0
(+)-isoxanthochymol

Guidance literature:: With hydrogenchloride; In benzene; for 3h; Yield given; Heating; further reagents: hydroiodic acid or trifluoracetic acid;

Reference yield:

: C₃₁H₄₆O₃

: (±)-isogarcinol

: 52617-33-1,71117-97-0
(+)-isoxanthochymol

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium tert-butylate / tetrahydrofuran / 0.75 h / 0 - 20 °C / Inert atmosphere; Schlenk technique

1.2: 48 h / 20 °C / Inert atmosphere; Schlenk technique

2.1: potassium carbonate / methanol / 2.5 h / 20 °C / Inert atmosphere; Schlenk technique

3.1: hydrogenchloride / toluene; water / 2 h / Inert atmosphere; Schlenk technique; Reflux

With hydrogenchloride; potassium tert-butylate; potassium carbonate; In tetrahydrofuran; methanol; water; toluene;
DOI:10.1002/chem.201406077