Baptigenin

Base Information

Chemical Name:Baptigenin
CAS No.:5908-63-4
Molecular Formula:C₁₅H₁₀O₆
Molecular Weight:286.241
Hs Code.:
UNII:NR2UM1NX6N
DSSTox Substance ID:DTXSID901318382
Wikidata:Q27285005
Metabolomics Workbench ID:22200
Mol file:5908-63-4.mol

Synonyms:Baptigenin;Baptigenin [MI];Tetrahydroxyisoflavone;UNII-NR2UM1NX6N;NR2UM1NX6N;5908-63-4;7-Hydroxy-3-(3,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one;4H-1-Benzopyran-4-one, 7-hydroxy-3-(3,4,5-trihydroxyphenyl)-;SCHEMBL555129;DTXSID901318382;7,3',4',5'-Tetrahydroxyisoflavon;7,3',4',5'-tetrahydroxyisoflavone;LMPK12050062;AKOS005166874;Isoflavone, 3',4',5',7-tetrahydroxy-;Q27285005

Suppliers and Price of Baptigenin

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

American Custom Chemicals Corporation
BAPTIGENIN 95.00%
5MG
$ 501.13

Total 0 raw suppliers

Chemical Property of Baptigenin

Chemical Property:

Vapor Pressure:0mmHg at 25°C
Melting Point:284-285°
Boiling Point:643.5°Cat760mmHg
Flash Point:250.1°C
PSA：111.13000
Density:1.654g/cm³
LogP:2.28240
XLogP3:1.8
Hydrogen Bond Donor Count:4
Hydrogen Bond Acceptor Count:6
Rotatable Bond Count:1
Exact Mass:286.04773803
Heavy Atom Count:21
Complexity:435

Purity/Quality:: BAPTIGENIN 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:C1=CC2=C(C=C1O)OC=C(C2=O)C3=CC(=C(C(=C3)O)O)O

Technology Process of Baptigenin

There total 6 articles about Baptigenin 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: 73.4%

: 98469-92-2
7-hydroxy-3-(3,4,5-trimethoxyphenyl)-4H-1-benzopyran-4-one

: 5908-63-4
3',4',5',7-tetrahydroxyisoflavone

Guidance literature:: With hydrogen iodide; for 2h; Heating;

Reference yield:

: 86-81-7
3,4,5-trimethoxy-benzaldehyde

: 5908-63-4
3',4',5',7-tetrahydroxyisoflavone

Guidance literature:: Multi-step reaction with 5 steps

1: 90.5 percent / 50percent aq. KOH / ethanol / 24 h / Ambient temperature

2: thallium nitrate / CHCl₃ / Ambient temperature

3: H₂, triethylamine / 10percent Pd/C / ethyl acetate / 760 Torr / Ambient temperature

4: 5percent HCl / methanol / 2 h / Heating

5: 73.4 percent / hydroiodic acid / 2 h / Heating

With hydrogenchloride; potassium hydroxide; thallium(I) nitrate; hydrogen iodide; hydrogen; triethylamine; palladium on activated charcoal; In methanol; ethanol; chloroform; ethyl acetate;

Reference yield:

: 148356-59-6
2',4'-bis(benzyloxy)-3,4,5-trimethoxychalcone

: 5908-63-4
3',4',5',7-tetrahydroxyisoflavone

Guidance literature:: Multi-step reaction with 4 steps

1: thallium nitrate / CHCl₃ / Ambient temperature

2: H₂, triethylamine / 10percent Pd/C / ethyl acetate / 760 Torr / Ambient temperature

3: 5percent HCl / methanol / 2 h / Heating

4: 73.4 percent / hydroiodic acid / 2 h / Heating

With hydrogenchloride; thallium(I) nitrate; hydrogen iodide; hydrogen; triethylamine; palladium on activated charcoal; In methanol; chloroform; ethyl acetate;