| 词条 | Helicin |
| 释义 |
| ImageFile = Helicin.png | ImageSize = 180px | IUPACName = | OtherNames = |Section1={{Chembox Identifiers | CASNo = 618-65-5 | PubChem = 101799 | ChemSpiderID = 91979 | KEGG = | SMILES = C1=CC=C(C(=C1)C=O)O[C@H]2[C@@H]([C@H]([C@@H]([C@H](O2)CO)O)O)O | InChI = 1S/C13H16O7/c14-5-7-3-1-2-4-8(7)19-13-12(18)11(17)10(16)9(6-15)20- 13/h1-5,9-13,15-18H,6H2/t9-,10-,11+,12-,13-/m1/s1 | InChIKey = BGOFCVIGEYGEOF-UJPOAAIJSA-N | StdInChI = | StdInChIKey = |Section2={{Chembox Properties | C=13 | H=16 | O=7 | Appearance = | Density = | MeltingPtC = | MeltingPt_notes = | BoilingPt = | Solubility = |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }}Helicin is the O-glucoside of salicylaldehyde.[1] References1. ^{{cite journal|last1=Zenk|first1=M.H.|title=Pathways of salicyl alcohol and salicin formation in Salix purpurea L.|journal=Phytochemistry|volume=6|issue=2|year=1967|pages=245–252|issn=0031-9422|doi=10.1016/S0031-9422(00)82770-3}} {{organic-compound-stub}} 2 : Phenol glucosides|Aldehydes |
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