Isobavachin

Base Information

Chemical Name:Isobavachin
CAS No.:31524-62-6
Molecular Formula:C20H20 O4
Molecular Weight:324.376
Hs Code.:2932999099
DSSTox Substance ID:DTXSID20953509
Nikkaji Number:J18.895F
Wikidata:Q72484945
ChEMBL ID:CHEMBL491534
Mol file:31524-62-6.mol

Synonyms:4',7-dihydroxy-8-prenylflavanone;isobavachin

Suppliers and Price of Isobavachin

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

DC Chemicals
Isobavachin >98%
20 mg
$ 380.00

Crysdot
Isobavachin 95+%
100mg
$ 400.00

Crysdot
Isobavachin 95+%
25mg
$ 150.00

Crysdot
Isobavachin 95+%
10mg
$ 85.00

Crysdot
Isobavachin 95+%
50mg
$ 250.00

Arctom
Isobavachin
20mg
$ 188.00

Arctom
Isobavachin ≥98%
100mg
$ 404.00

American Custom Chemicals Corporation
ISOBAVACHIN 95.00%
5MG
$ 500.05

Total 43 raw suppliers

Chemical Property of Isobavachin

Chemical Property:

Vapor Pressure:4.52E-13mmHg at 25°C
Melting Point:187-188℃
Boiling Point:558.3°C at 760 mmHg
Flash Point:202.1°C
PSA：66.76000
Density:1.244
LogP:4.31300
Storage Temp.:2-8°C
XLogP3:4.1
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:3
Exact Mass:324.13615911
Heavy Atom Count:24
Complexity:474

Purity/Quality:

≥98% ^*data from raw suppliers

Isobavachin >98% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:CC(=CCC1=C(C=CC2=C1OC(CC2=O)C3=CC=C(C=C3)O)O)C
Isomeric SMILES:CC(=CCC1=C(C=CC2=C1O[C@@H](CC2=O)C3=CC=C(C=C3)O)O)C
Uses Flavonoids is the parent compound for I315240. Flavonoids are ant-idiabetic activity, most of the flavonoids showed a remarkable in vitro activity.

Technology Process of Isobavachin

There total 1 articles about Isobavachin 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: 45.8%

: 358-72-5
dimethylallyl diphosphate

: 578-86-9,41680-09-5
liquiritigenin

: 31524-62-6
((2S)-2,3-dihydro-7-hydroxy-2-hydroxyphenyl)-8-(3-methyl-2-buten-1-yl)-4H-1-benzopyran-4-one

Guidance literature:: With recombinant Sophora flavescens flavonoid prenyltransferase; magnesium chloride; In aq. buffer; at 40 ℃; for 2h; pH=9; stereospecific reaction; Kinetics; Enzymatic reaction;
DOI:10.1002/adsc.201300196