| Weight | 207.252 g/mol |
|---|---|
| Formula | C15H11O+ |
| Hydrogen Acceptors | 0 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 3 |
| Rotatable Bonds | 1 |
Flavylium (11029-12-2)
Score:
#1660 in Physics
,
#5106 in Chemistry
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- Sigma-Aldrich - Search for Flavylium
- Fisher Scientific - Search for Flavylium
- TCI - Search for Flavylium
- The chemistry of anthocyanins, anthocyanidins and related flavylium salts (Tetrahedron, 1983)
- Chemistry and applications of flavylium compounds: a handful of colours (Chemical Society Reviews, 2012)
- Hydration of the flavylium ion (Journal of the American Chemical Society, 1980)
- Coupling reactions between flavylium ions and catechin (Phytochemistry, 1996)
- Kinetic and thermodynamic control of flavylium hydration in the pelargonidin-cinnamic acid complexation. Origin of the extraordinary flower color diversity of Pharbitis nil (Journal of the American Chemical Society, 1993)
- Multistate/Multifunctional Molecular-Level Systems: Light and pH Switching between the Various Forms of a Synthetic Flavylium Salt (Chemistry: A European Journal, 1998)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CC=C(C=C1)C2=[O+]C3=CC=CC=C3C=C2
-
InChIKeyNWKFECICNXDNOQ-UHFFFAOYSA-N
- Pubchem - Flavylium
- Wikipedia - Anthocyanidins
Anthocyanidins are common plant pigments. They are the sugar-free counterparts of anthocyanins based on the flavylium ion or 2-phenylchromenylium, which is a type of oxonium ion (chromenylium is referred also to as benzopyrylium). They form a large group of polymethine dye.
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