5-O-Methylmyricetin

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5-O-Methylmyricetin
Chemical structure of 5-O-methylmyricetin 5-O-Methylmyricetin.svg
Chemical structure of 5-O-methylmyricetin
Names
IUPAC name
3,3′,4′,5′,7-Pentahydroxy-5-methoxyflavone
Systematic 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
PubChem CID
  • 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 Yes check.svgY
    Key: DDVGNSDGGWHPQZ-UHFFFAOYSA-N Yes check.svgY
  • 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).
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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. [1]

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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