7,8-Dihydroxy-4'-methoxyisoflavone

• CAS: 480-86-4
• Catalog Number: ACM480864
• Category: Other Products
• Molecular Weight: 311.37
• Molecular Formula: C₁₆H₁₂O₅
• Synonyms: 8-Hydroxyformononetin
• InChI: InChI=1S/C16H25NO5/c1-9-10(2)16(3,20)15(19)21-8-11-4-6-17-7-5-12(13(11)17)22-14(9)18/h9-13,20H,4-8H2,1-3H3/t9-,10+,11+,12-,13-,16-/m1/s1
• InChI Key: GXAPLLMJHZBIPX-VZYPABODSA-N
• Complexity: 481
• Covalently-Bonded Unit Count: 1
• Defined Atom Stereocenter Count: 6
• Exact Mass: 311.1732729
• Heavy Atom Count: 22
• Hydrogen Bond Acceptor Count: 6
• Hydrogen Bond Donor Count: 1
• Isomeric SMILES: C[C@@H]1[C@@H]([C@@](C(=O)OC[C@@H]2CCN3[C@H]2[C@@H](CC3)OC1=O)(C)O)C
• Monoisotopic Mass: 311.1732729
• Physical State: Powder
• Rotatable Bond Count: 0
• Topological Polar Surface Area: 76.1 Ų

Custom Q&A

What is the chemical name of the compound with the synonym 8'-HYDROXYFORMONONETIN?

The chemical name of the compound is 7,8-DIHYDROXY-4'-METHOXYISOFLAVONE.

What is the molecular formula of 7,8-DIHYDROXY-4'-METHOXYISOFLAVONE?

The molecular formula is C16H25NO5.

What is the molecular weight of 7,8-DIHYDROXY-4'-METHOXYISOFLAVONE?

The molecular weight is 311.37 g/mol.

What is the CAS number of 7,8-DIHYDROXY-4'-METHOXYISOFLAVONE?

The CAS number is 480-86-4.

What are some other synonyms for 7,8-DIHYDROXY-4'-METHOXYISOFLAVONE?

Other synonyms include RETUSIN, RETUSINE, and Aids071726.

What is the chemical structure of 7,8-DIHYDROXY-4'-METHOXYISOFLAVONE?

The chemical structure is a 4H-1-Benzopyran-4-one with 2-(3,4-dimethoxyphenyl)-5-hydroxy-3,7-dimethoxy-.

What are some potential applications or uses of 7,8-DIHYDROXY-4'-METHOXYISOFLAVONE?

It may have potential uses in research, pharmaceuticals, or cosmetics.

Are there any known side effects or risks associated with 7,8-DIHYDROXY-4'-METHOXYISOFLAVONE?

It is always recommended to consult with a healthcare professional before using any new compound.

How is 7,8-DIHYDROXY-4'-METHOXYISOFLAVONE typically obtained or synthesized?

The compound may be obtained through synthesis in a laboratory setting.