词条 | Anhalinine |
释义 |
| ImageFile = Anhalinine.svg | ImageSize = 150px | IUPACName = 6,7,8-Trimethoxy-1,2,3,4-tetrahydroisoquinoline | OtherNames = |Section1={{Chembox Identifiers | CASNo = 642-30-8 | PubChem = 192723 | ChemSpiderID = 167242 | SMILES = COC1=C(C(=C2CNCCC2=C1)OC)OC | InChI = 1/C12H17NO3/c1-14-10-6-8-4-5-13-7-9(8)11(15-2)12(10)16-3/h6,13H,4-5,7H2,1-3H3 | InChIKey = GOBKARNYNSWQFZ-UHFFFAOYAR | StdInChI = 1S/C12H17NO3/c1-14-10-6-8-4-5-13-7-9(8)11(15-2)12(10)16-3/h6,13H,4-5,7H2,1-3H3 | StdInChIKey = GOBKARNYNSWQFZ-UHFFFAOYSA-N |Section2={{Chembox Properties | Formula = C12H17NO3 | MolarMass = 223.268 | Appearance = | Density = | MeltingPtC = 60-61 | MeltingPt_ref =[1] | BoilingPtC = 144-145 | BoilingPt_ref =[1] | BoilingPt_notes = at 0.1 Torr | Solubility = |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} Anhalinine is a naturally occurring bio-active alkaloid[2] which can be isolated from Lophophora williamsii. It is structurally related to Mescaline. See also
References1. ^1 {{cite journal|last1=Taylor|first1=E. P.|title=236. Synthetic neuromuscular blocking agents. Part III. Miscellaneous quaternary ammonium salts|journal=Journal of the Chemical Society (Resumed)|date=1952|pages=1309|doi=10.1039/jr9520001309}} {{organic-chem-stub}}2. ^{{cite journal|last1=Ghansah|first1=E.|last2=Kopsombut|first2=P.|last3=Maleque|first3=M.A.|last4=Brossi|first4=A.|title=Effects of mescaline and some of its analogs on cholinergic neuromuscular transmission|journal=Neuropharmacology|date=February 1993|volume=32|issue=2|pages=169–174|doi=10.1016/0028-3908(93)90097-M}} 1 : Lophophora |
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