| 词条 | 5-O-Methylmyricetin |
| 释义 |
| Watchedfields = changed | verifiedrevid = 477225433 | Name = 5-O-Methylmyricetin | ImageFile = 5-O-methylmyricetin.PNG | ImageName = Chemical structure of 5-O-methylmyricetin | IUPACName = 3,7-dihydroxy-5-methoxy-2-(3,4,5-trihydroxyphenyl)chromen-4-one | OtherNames = 5-Methylmyricetin |Section1={{Chembox Identifiers | 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 | InChIKey = DDVGNSDGGWHPQZ-UHFFFAOYAT | SMILES1 = O=C1c3c(O/C(=C1/O)c2cc(O)c(O)c(O)c2)cc(O)cc3OC | StdInChI_Ref = {{stdinchicite|correct|chemspider}} | StdInChI = 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 | StdInChIKey_Ref = {{stdinchicite|correct|chemspider}} | StdInChIKey = DDVGNSDGGWHPQZ-UHFFFAOYSA-N | CASNo = | CASNo_Ref = | CASNoOther = | ChemSpiderID_Ref = {{chemspidercite|correct|chemspider}} | ChemSpiderID = 4477964 | PubChem = 5319731 | SMILES = COC1=C2C(=CC(=C1)O)OC(=C(C2=O)O)C3=CC(=C(C(=C3)O)O)O | MeSHName = }} |Section2={{Chembox Properties | Formula = C16H12O8 | MolarMass = 332.26 g/mol | Appearance = | Density = 1.731 g/mL | MeltingPt = | BoilingPt = | Solubility = }} }} 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] References1. ^{{cite journal | url = http://www.springerlink.com/content/u836k7100hq55233 | title = Synthesis of naturally occurring partial methyl ethers of myricetin | author = P. N. Sarma, G. Srimannarayana and N. V. Subba Rao | journal = Proceedings Mathematical Sciences | volume = 80 | issue = 4 | year = 1974}} {{flavonol}}{{DEFAULTSORT:Methylmyricetin, 5-O-}}{{Natural-phenol-stub}} 2 : O-Methylated flavonols|Pyrogallols |
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