Levorphanol

Base Information Edit

Chemical Name:Levorphanol
CAS No.:77-07-6
Deprecated CAS:125-74-6
Molecular Formula:C₁₇H₂₃NO
Molecular Weight:257.376
Hs Code.:
European Community (EC) Number:206-048-0,201-002-6
UNII:27618J1N2X,V7R79HN3XD
DSSTox Substance ID:DTXSID3023213,DTXSID301016136
Wikipedia:Levorphanol,Racemorphan
Wikidata:Q2579108
NCI Thesaurus Code:C61810,C152138
RXCUI:6378
Pharos Ligand ID:1U43KCX12F39
Metabolomics Workbench ID:43134
ChEMBL ID:CHEMBL592
Mol file:77-07-6.mol

Synonyms:3 Hydroxy N methylmorphinan;3-Hydroxy-N-methylmorphinan;L Dromoran;L-Dromoran;Levo Dromoran;Levo-Dromoran;Levodroman;LevoDromoran;Levorphan;Levorphanol;Levorphanol Tartrate;Tartrate, Levorphanol

This product is a nationally controlled contraband, and the Lookchem platform doesn't provide relevant sales information.

Chemical Property of Levorphanol Edit

Chemical Property:

Vapor Pressure:2.55E-07mmHg at 25°C
Melting Point:198-199°
Refractive Index:1.5200 (estimate)
Boiling Point:410.4°Cat760mmHg
PKA:10.07±0.20(Predicted)
Flash Point:207.2°C
PSA：23.47000
Density:1.17g/cm³
LogP:3.01830
XLogP3:3.1
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:2
Rotatable Bond Count:0
Exact Mass:257.177964357
Heavy Atom Count:19
Complexity:357

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Drug Classes:Opioids
Canonical SMILES:CN1CCC23CCCCC2C1CC4=C3C=C(C=C4)O
Isomeric SMILES:CN1CC[C@]23CCCC[C@H]2[C@H]1CC4=C3C=C(C=C4)O
Recent ClinicalTrials:Levorphanol as a Second Line Opioid in Reducing Pain in Patients With Cancer
Uses Levorphanol is an intermediate in the synthesis of Levorphanol L-Tartrate(L376500). Levorphanol Tartrate is an orally active synthetic morphine analog. Analgesic (narcotic). Controlled substance.

Technology Process of Levorphanol

There total 39 articles about Levorphanol which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 100.0%