Robinetinidin - Misplaced Pages

This is the current revision of this page, as edited by Innerstream (talk | contribs) at 00:23, 28 January 2022. The present address (URL) is a permanent link to this version.

Revision as of 00:23, 28 January 2022 by Innerstream (talk | contribs)(diff) ← Previous revision | Latest revision (diff) | Newer revision → (diff)

Robinetinidin
Names
Chemical structure of robinetinidin
IUPAC name 5-(3,7-Dihydroxychromenylium-2-yl)benzene-1,2,3-triol chloride
Other names 3,3',4',5',7-Pentahydroxyflavylium chloride
Identifiers
CAS Number	3020-09-5
3D model (JSmol)	Interactive image
ChemSpider	21489630
PubChem CID	16212723
UNII	DW6W3V57N8
CompTox Dashboard (EPA)	DTXSID80583684
InChI InChI=1S/C15H10O6/c16-9-2-1-7-3-12(19)15(21-13(7)6-9)8-4-10(17)14(20)11(18)5-8/h1-6H,(H4-,16,17,18,19,20)/p+1Key: BQLHYJCUNNPCKQ-UHFFFAOYSA-O InChI=1/C15H10O6/c16-9-2-1-7-3-12(19)15(21-13(7)6-9)8-4-10(17)14(20)11(18)5-8/h1-6H,(H4-,16,17,18,19,20)/p+1Key: BQLHYJCUNNPCKQ-IKLDFBCSAA
SMILES C1=CC(=CC2=C(=C(C=C21)O)C3=CC(=C(C(=C3)O)O)O)O.
Properties
Chemical formula	C₁₅H₁₁ClO₆ (C₁₅H₁₁O₆, Cl)
Molar mass	322.69 g/mol
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). N verify (what is ?) Infobox references

Chemical compound

Robinetinidin is an anthocyanidin, a type of flavonoid.

Prorobinetinidins, condensed tannins oligomers containing robinetinidol, can be found in Stryphnodendron adstringens. They yield robinetinidin when depolymerized under oxidative conditions.

References

Prorobinetinidins from Stryphnodendron adstringens. Palazzo de Mello J.; Petereit F.; Nahrstedt A., Phytochemistry, 1996.

Acetylated anthocyanins	Cyanidin 3-O-(6-acetyl)glucoside Delphinidin 3-O-(6-acetyl)glucoside Malvidin 3-O-(6-acetyl)glucoside Petunidin 3-O-(6-acetyl)galactoside Petunidin 3-O-(6-acetyl)glucoside Peonidin 3-O-(6-acetyl)glucoside
Coumaroylated anthocyanins (cis- and trans-)	Cyanidin 3-O-(6-p-coumaroyl)glucoside Delphinidin 3-O-(6-p-coumaroyl)glucoside Malvidin 3-O-(6-p-coumaroyl)glucoside Petunidin 3-O-(6-p-coumaroyl)glucoside Peonidin 3-O-(6-p-coumaroyl)glucoside
Caffeoylated anthocyanins	Malvidin 3-O-(6-p-caffeoyl)glucoside Peonidin 3-O-(6-p-caffeoyl)glucoside
Malonylated anthocyanins	Malonylmalvin (malvidin 3-(6″-malonylglucoside)-5-glucoside)
Acylated anthocyanin diglycosides	Cyanidin 3-O-(di-p-coumarylglucoside)-5-glucoside Gentiodelphin (delphinidin 3-''O''-glucosyl-5-''O''-(6-''O''-caffeoyl-glucosyl)-3′-''O''-(6-''O''-caffeoyl-glucoside)) Nasunin (Delphinidin 3-(p-coumaroylrutinoside)-5-glucoside) Petanin (petunidin 3--5-O-β-D-glucopyranoside) Violdelphin (Delphinidin 3-rutinoside-7-O-(6-O-(4-(6-O-(4-hydroxybenzoyl)-β-D-glucosyl)oxybenzoyl)-β-D-glucoside)

Flavanol-anthocyanin adducts

Miscellaneous

Metalloanthocyanins (commelinin)
Cyanosalvianin
Protocyanin
Protodelphin)
Pyranoanthocyanins
Copigmentation
Anthocyanone A (degradation product of oenin)
Malvone (oxidation product of malvin)

This article about an aromatic compound is a stub. You can help Misplaced Pages by expanding it.

Categories:

References

See also