5-O-Methylmyricetin

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 synthetized.[1]

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
3D model (JSmol)
ChEMBL
ChemSpider
  • 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,1H3 Y
    Key: DDVGNSDGGWHPQZ-UHFFFAOYSA-N Y
  • 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,1H3
    Key: DDVGNSDGGWHPQZ-UHFFFAOYAT
  • 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
C16H12O8
Molar mass 332.264 g·mol−1
Density 1.731 g/mL
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)
Infobox references

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.
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