Dihydroformononetin

Base Information

• Chemical Name: Dihydroformononetin
• CAS No.: 4626-22-6
• Molecular Formula: C16H14 O4
• Molecular Weight: 270.285
• ChEMBL ID: CHEMBL3343011
• DSSTox Substance ID: DTXSID401175698
• Metabolomics Workbench ID: 22585
• Nikkaji Number: J2.107.844A
• Wikidata: Q104398913
• Mol file: 4626-22-6.mol

Synonyms:Dihydroformononetin;4626-22-6;7-Hydroxy-4'-methoxyisoflavanone;7-hydroxy-3-(4-methoxyphenyl)-2,3-dihydrochromen-4-one;CHEMBL3343011;7-hydroxy-3-(4-methoxyphenyl)-3,4-dihydro-2H-1-benzopyran-4-one;SCHEMBL2069507;CHEBI:174556;INYISIYHXQDCPK-UHFFFAOYSA-N;DTXSID401175698;BDBM50102651;LMPK12050448;2,3-Dihydro-7-hydroxy-3-(4-methoxyphenyl)-4H-1-benzopyran-4-one

Chemical Property of Dihydroformononetin

Chemical Property:

• PSA: 55.76000
• LogP: 2.75970
• XLogP3: 2.7
• Hydrogen Bond Donor Count: 1
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 270.08920892
• Heavy Atom Count: 20
• Complexity: 348

Purity/Quality:

99% ^*data from raw suppliers

Dihydroformononetin ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: COC1=CC=C(C=C1)C2COC3=C(C2=O)C=CC(=C3)O

Technology Process of Dihydroformononetin

There total 11 articles about Dihydroformononetin 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: 93.0%

7-ethoxymethoxy-4'-methoxyisoflavanone (97714-86-8) → Dihydroformononetin (4626-22-6)

Guidance literature:

With hydrogenchloride; In methanol; for 0.166667h;

Reference yield: 90.0%

7-Hydroxy-3-(4-methoxy-phenyl)-chromen-4-on (485-72-3) → Dihydroformononetin (4626-22-6) + trans-7-hydroxy-4'-methoxyisoflavan-4-ol (124093-20-5)

Guidance literature:

With ammonium formate; palladium on activated charcoal; In methanol; Ambient temperature;

Reference yield: 90.0%

7-benzyloxy-3-(4-methoxyphenyl)-3H-benzopyran-4-one (10499-15-7) → Dihydroformononetin (4626-22-6)

Guidance literature:

With 5%-palladium/activated carbon; In tetrahydrofuran; at 20 ℃;

DOI:10.1016/j.jsbmb.2016.01.010

upstream raw materials:

7-Hydroxy-3-(4-methoxy-phenyl)-chromen-4-on

3,4-dihydro-7-hydroxy-3-(4-methoxyphenyl)-2H-1-benzopyran

7-ethoxymethoxy-4'-methoxyisoflavanone

1-(2,4-dihydroxyphenyl)-2-(4-methoxyphenyl)ethanone

Downstream raw materials:

4'-methoxy-6'',6''-dimethylpyrano<2'',3'':7,8>isoflavanone

C₂₀H₂₃NO₄

C₂₃H₂₉NO₄

C₁₉H₂₁NO₄

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