Misplaced Pages

This is an old revision of this page, as edited by Graeme Bartlett (talk | contribs) at 22:43, 22 January 2023 (synthetized fix). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

5-O-Methylmyricetin

Names
IUPAC name 3,3′,4′,5′,7-Pentahydroxy-5-methoxyflavone
Preferred IUPAC name 3,7-Dihydroxy-5-methoxy-2-(3,4,5-trihydroxyphenyl)-4H-1-benzopyran-4-one
Other names 5-Methylmyricetin
Identifiers
CAS Number	19077-84-0
3D model (JSmol)	Interactive image Interactive image
ChEMBL	ChEMBL4470965
ChemSpider	4477964
PubChem CID	5319731
CompTox Dashboard (EPA)	DTXSID201029314
InChI InChI=1S/C16H12O8/c1-23-10-4-7(17)5-11-12(10)14(21)15(22)16(24-11)6-2-8(18)13(20)9(19)3-6/h2-5,17-20,22H,1H3Key: DDVGNSDGGWHPQZ-UHFFFAOYSA-N InChI=1/C16H12O8/c1-23-10-4-7(17)5-11-12(10)14(21)15(22)16(24-11)6-2-8(18)13(20)9(19)3-6/h2-5,17-20,22H,1H3Key: DDVGNSDGGWHPQZ-UHFFFAOYAT
SMILES COC1=C2C(=CC(=C1)O)OC(=C(C2=O)O)C3=CC(=C(C(=C3)O)O)O O=C1c3c(O/C(=C1/O)c2cc(O)c(O)c(O)c2)cc(O)cc3OC
Properties
Chemical formula	C16H12O8
Molar mass	332.264 g·mol
Density	1.731 g/mL
Except where otherwise noted, data are given for materials in their standard state (at 25 °C , 100 kPa). Y verify (what is  ?) Infobox references

5-O-Methylmyricetin is an O-methylated flavonol, a type of flavonoid. It is the 5-O-methyl derivative of myricetin. It occurs naturally and can also be synthesized.

References

1. P. N. Sarma, G. Srimannarayana and N. V. Subba Rao (1974). "Synthesis of naturally occurring partial methyl ethers of myricetin". Proceedings Mathematical Sciences. 80 (4): 168–173. doi:10.1007/BF03046674. S2CID 92325935.

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

• v
• t
• e

• O-methylated flavonols
• Pyrogallols
• Aromatic compound stubs