| 词条 | Isomethadol |
| 释义 |
| ImageFile = isomethadol.svg | ImageSize = | IUPACName = 6-(Dimethylamino)-5-methyl-4,4-diphenyl-3-hexanol | OtherNames = |Section1={{Chembox Identifiers | CASNo = 25117-79-7 | PubChem = 44676 | ChemSpiderID = 40651 | SMILES = OC(C(c1ccccc1)(c2ccccc2)C(C)CN(C)C)CC | InChI = 1/C21H29NO/c1-5-20(23)21(17(2)16-22(3)4,18-12-8-6-9-13-18)19-14-10-7-11-15-19/h6-15,17,20,23H,5,16H2,1-4H3 | InChIKey = UKKMLFPHCPRNJI-UHFFFAOYAF | StdInChI = 1S/C21H29NO/c1-5-20(23)21(17(2)16-22(3)4,18-12-8-6-9-13-18)19-14-10-7-11-15-19/h6-15,17,20,23H,5,16H2,1-4H3 | StdInChIKey = UKKMLFPHCPRNJI-UHFFFAOYSA-N |Section2={{Chembox Properties | Formula = C21H29NO | MolarMass = 311.461 | Appearance = | Density = | MeltingPtC = 125 to 126 | MeltingPt_ref = [1] | BoilingPt = | Solubility = |Section3={{Chembox Hazards | MainHazards = | FlashPt = | AutoignitionPt = }} Isomethadol is a opioid analgesic with a number of stereoisomers (viz. alpha and beta forms of dextro, laevo, and racemic isomers for a total of six) produced by the reduction of d,l-isomethadone with lithium aluminium hydride.[2] It was first produced in the United States in 1948. The salt used in research is the hydrochloride. References1. ^{{cite journal|last1=May|first1=Everette L.|last2=Eddy|first2=Nathan B.|title=The Isomethadols and their Acetyl Derivatives|journal=The Journal of Organic Chemistry|volume=17|issue=9|year=1952|pages=1210–1215|issn=0022-3263|doi=10.1021/jo50009a005}} {{Opioidergics}}{{analgesic-stub}}2. ^Merck Index, 11th edition, 5068 1 : Opioids |
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