Isomedicarpin

Base Information

Chemical Name:Isomedicarpin
CAS No.:74560-05-7
Molecular Formula:C₁₆H₁₄O₄
Molecular Weight:270.285
Hs Code.:
Metabolomics Workbench ID:22756
Nikkaji Number:J1.904.410F
Wikidata:Q110204701
Mol file:74560-05-7.mol

Synonyms:Isomedicarpin;9-Hydroxy-3-methoxypterocarpan;3-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-9-ol;(6aR,11aR)-3-methoxy-6a,11a-dihydro-6H-[1]benzofuro[3,2-c]chromen-9-ol;SCHEMBL12912390;LMPK12070030

Suppliers and Price of Isomedicarpin

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
Isomedicarpin 95+%
5mg
$ 860.00

Arctom
Isomedicarpin ≥98%
5mg
$ 553.00

American Custom Chemicals Corporation
9-HYDROXY-3-METHOXYPTEROCARPIN 95.00%
5MG
$ 504.98

Total 14 raw suppliers

Chemical Property of Isomedicarpin

Chemical Property:

PSA：47.92000
LogP:3.01050
XLogP3:2.6
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:1
Exact Mass:270.08920892
Heavy Atom Count:20
Complexity:360

Purity/Quality:

98% ^*data from raw suppliers

Isomedicarpin 95+% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC2=C(C=C1)C3C(CO2)C4=C(O3)C=C(C=C4)O

Technology Process of Isomedicarpin

There total 8 articles about Isomedicarpin 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: 61.3%

: 101383-15-7,112639-50-6
4-(3,4-dihydro-cis-4-hydroxy-7-methoxy-2H-1-benzopyran-3-yl)-1,3-benzenediol

: 38822-00-3,74560-05-7,129262-45-9
dl-isomedicarpin

Guidance literature:: In acetic acid; for 1h; Heating;

Reference yield:

: 30779-83-0
3,4-dihydro-7-methoxy-4-oxo-2H-1-benzopyran-3-acetic acid

: 38822-00-3,74560-05-7,129262-45-9
dl-isomedicarpin

Guidance literature:: Multi-step reaction with 5 steps

1: 72.9 percent

2: 78.8 percent

3: 78.5 percent / MCPBA (70percent) / CH₂Cl₂ / 2 h / 0 °C

4: 1.) magnesium methoxide / 1.) methanol, rt., 16 h; 2.) benzene, reflux, 3 h

5: 61.3 percent / acetic acid / 1 h / Heating

With magnesium methanolate; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; acetic acid;

Reference yield:

: 80930-46-7
3-bromo-2,3-dihydro-7-methoxy-4H-1-benzopyran-4-one

: 38822-00-3,74560-05-7,129262-45-9
dl-isomedicarpin

Guidance literature:: Multi-step reaction with 7 steps

2: 58.7 percent

3: 72.9 percent

4: 78.8 percent

5: 78.5 percent / MCPBA (70percent) / CH₂Cl₂ / 2 h / 0 °C

6: 1.) magnesium methoxide / 1.) methanol, rt., 16 h; 2.) benzene, reflux, 3 h

7: 61.3 percent / acetic acid / 1 h / Heating

With magnesium methanolate; 3-chloro-benzenecarboperoxoic acid; In dichloromethane; acetic acid;