Lotisoflavan

Base Information

Chemical Name:Lotisoflavan
CAS No.:77370-02-6
Molecular Formula:C₁₇H₁₈O₅
Molecular Weight:302.327
Hs Code.:
DSSTox Substance ID:DTXSID90331956
Nikkaji Number:J2.773.266F
Wikidata:Q27107235
Metabolomics Workbench ID:22933

Synonyms:Lotisoflavan;77370-02-6;2',4'-Dihydroxy-5,7-dimethoxyisoflavan;4-(5,7-dimethoxy-3,4-dihydro-2H-chromen-3-yl)benzene-1,3-diol;CHEBI:6543;DTXSID90331956;LMPK12080048;XL161806;Q27107235;4-(5,7-dimethoxy-3,4-dihydro-2H-1-benzopyran-3-yl)benzene-1,3-diol

Suppliers and Price of Lotisoflavan

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 0 raw suppliers

Chemical Property of Lotisoflavan

Chemical Property:

Vapor Pressure:1.28E-10mmHg at 25°C
Boiling Point:500°C at 760 mmHg
Flash Point:256.2°C
Density:1.279g/cm³
XLogP3:2.9
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:5
Rotatable Bond Count:3
Exact Mass:302.11542367
Heavy Atom Count:22
Complexity:363

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Canonical SMILES:COC1=CC2=C(CC(CO2)C3=C(C=C(C=C3)O)O)C(=C1)OC

Technology Process of Lotisoflavan

There total 4 articles about Lotisoflavan 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:

: 5,7-dimethoxy-2',4'-dibenzyloxyisoflavone

: 77370-02-6
lotisoflavan

Guidance literature:: With hydrogen; palladium on activated charcoal; In acetic acid; Ambient temperature;
DOI:10.1016/S0031-9422(00)83980-1

Reference yield:

: 77370-33-3
2,4-dibenzyloxy-2'-hydroxy-4',6'-dimethoxychalcone

: 77370-02-6
lotisoflavan

Guidance literature:: Multi-step reaction with 3 steps

1: pyridine / Ambient temperature

2: 1., Tl(NO₃)2*3H₂O; 2.) KOH; 3.) 10percent HCl / 1.) MeOH, RT; 2.) 1 h; 3.) reflux, 1.5 h

3: 65 mg / H₂ / 10percent Pd/C / acetic acid / Ambient temperature

With hydrogenchloride; potassium hydroxide; Tl(NO₃)2*3H₂O; hydrogen; palladium on activated charcoal; In pyridine; acetic acid;
DOI:10.1016/S0031-9422(00)83980-1

Reference yield:

: 77370-34-4
Acetic acid 2-[(E)-3-(2,4-bis-benzyloxy-phenyl)-acryloyl]-3,5-dimethoxy-phenyl ester

: 77370-02-6
lotisoflavan

Guidance literature:: Multi-step reaction with 2 steps

1: 1., Tl(NO₃)2*3H₂O; 2.) KOH; 3.) 10percent HCl / 1.) MeOH, RT; 2.) 1 h; 3.) reflux, 1.5 h

2: 65 mg / H₂ / 10percent Pd/C / acetic acid / Ambient temperature

With hydrogenchloride; potassium hydroxide; Tl(NO₃)2*3H₂O; hydrogen; palladium on activated charcoal; In acetic acid;
DOI:10.1016/S0031-9422(00)83980-1