Structure via PubChem · Public domain (PubChem)
(2S)-flavan-4-ol
Sign in to saveAlso known as (2S)-2-phenylchroman-4-ol
The flavan-4-ols (3-deoxyflavonoids) are flavone-derived alcohols and a family of flavonoids. Flavan-4-ols are colorless precursor compounds that polymerize to form red phlobaphene pigments. They can be found in the sorghum. Glycosides (abacopterins A, B, C and D together with triphyllin A and 6,8-dimethyl-7-hydroxy-4‘-methoxyanthocyanidin-5-O-β-d-glucopyranoside) can be isolated from a methanol extract of the rhizomes of Abacopteris penangiana.
Chemical data
- Formula
- C15H14O2
- Molecular weight
- 226.27 g/mol
- IUPAC name
- (2S)-2-phenyl-3,4-dihydro-2H-chromen-4-ol
- SMILES
- C1[C@H](OC2=CC=CC=C2C1O)C3=CC=CC=C3
- InChIKey
- YTMFRMLVZQOBDR-WUJWULDRSA-N
- XLogP
- 2.7
- Polar surface area
- 29.5 Ų
- H-bond donors
- 1
- H-bond acceptors
- 2
- Formal charge
- 0
via PubChem
Wikidata facts
- Mass
- 226.09938
Show 3 more facts
- chemical formula
- C₁₅H₁₄O₂
- canonical SMILES
- C1C(C2=CC=CC=C2OC1C3=CC=CC=C3)O
- isomeric SMILES
- C1[C@H](OC2=CC=CC=C2C1O)C3=CC=CC=C3
Sources (1)
via Wikidata · CC0
~1 min read
Encyclopedic overview
4 sectionsContents
- Known flavan-4-ols
- Metabolism
- Spectral data
- References
The flavan-4-ols (3-deoxyflavonoids) are flavone-derived alcohols and a family of flavonoids. Flavan-4-ols are colorless precursor compounds that polymerize to form red phlobaphene pigments. They can be found in the sorghum. Glycosides (abacopterins A, B, C and D together with triphyllin A and 6,8-dimethyl-7-hydroxy-4‘-methoxyanthocyanidin-5-O-β-d-glucopyranoside) can be isolated from a methanol extract of the rhizomes of Abacopteris penangiana.
==Known flavan-4-ols== Apiforol Luteoforol
Excerpted from Wikipedia’s “(2S)-flavan-4-ol” article, available under the CC BY-SA 4.0 licence.