Asebogenin

Base Information

Chemical Name:Asebogenin
CAS No.:520-42-3
Molecular Formula:C16H16O5
Molecular Weight:288.3
Hs Code.:2914509090
DSSTox Substance ID:DTXSID60331781
Nikkaji Number:J367.549A
Wikidata:Q27105855
Metabolomics Workbench ID:27020
ChEMBL ID:CHEMBL253257
Mol file:520-42-3.mol

Synonyms:2',6',4-trihydroxy-4'-methoxydihydrochalcone;asebogenin

Suppliers and Price of Asebogenin

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

Crysdot
Asebogenin 95+%
5mg
$ 723.00

Total 10 raw suppliers

Chemical Property of Asebogenin

Chemical Property:

Vapor Pressure:9.53E-13mmHg at 25°C
Melting Point:168℃
Boiling Point:550.9°Cat760mmHg
PKA:7.00±0.40(Predicted)
Flash Point:207.6°C
PSA：86.99000
Density:1.325g/cm³
LogP:2.62750
XLogP3:3
Hydrogen Bond Donor Count:3
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:5
Exact Mass:288.09977361
Heavy Atom Count:21
Complexity:326

Purity/Quality:

98%Min ^*data from raw suppliers

Asebogenin 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC(=C(C(=C1)O)C(=O)CCC2=CC=C(C=C2)O)O

Technology Process of Asebogenin

There total 9 articles about Asebogenin 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:

: 2,6-diisopropyloxy-4-methoxyacetophenone

: 520-42-3
asebogenin

Guidance literature:: Multi-step reaction with 3 steps

1: 0.7 g

2: 0.5 g / H₂ / Pd-C / ethyl acetate / 3 h

3: 0.3 g / BCl₃ / CH₂Cl₂ / -70 deg C then warming to r.t

With hydrogen; boron trichloride; palladium on activated charcoal; In dichloromethane; ethyl acetate;
DOI:10.1016/S0031-9422(00)81760-4

Reference yield:

: 2',4,6'-triisopropyloxy-4'-methoxychalcone

: 520-42-3
asebogenin

Guidance literature:: Multi-step reaction with 2 steps

1: 0.5 g / H₂ / Pd-C / ethyl acetate / 3 h

2: 0.3 g / BCl₃ / CH₂Cl₂ / -70 deg C then warming to r.t

With hydrogen; boron trichloride; palladium on activated charcoal; In dichloromethane; ethyl acetate;
DOI:10.1016/S0031-9422(00)81760-4

Reference yield:

: 18962-05-5
4-isopropoxybenzaldehyde

: 520-42-3
asebogenin

Guidance literature:: Multi-step reaction with 3 steps

1: 0.7 g

2: 0.5 g / H₂ / Pd-C / ethyl acetate / 3 h

3: 0.3 g / BCl₃ / CH₂Cl₂ / -70 deg C then warming to r.t

With hydrogen; boron trichloride; palladium on activated charcoal; In dichloromethane; ethyl acetate;
DOI:10.1016/S0031-9422(00)81760-4