Ethylmorphine

Base Information Edit

Chemical Name:Ethylmorphine
CAS No.:76-58-4
Molecular Formula:C₁₉H₂₃NO₃
Molecular Weight:313.397
Hs Code.:
European Community (EC) Number:200-970-7
UNII:RWO67D87EU
DSSTox Substance ID:DTXSID1046760
Nikkaji Number:J4.179C
Wikipedia:Ethylmorphine
Wikidata:Q554881
NCI Thesaurus Code:C83704
Metabolomics Workbench ID:43565
ChEMBL ID:CHEMBL1712170
Mol file:76-58-4.mol

Synonyms:Dionine;Ethomorphine;Ethylmorphine;Ethylmorphine Hydrochloride, (5alpha,6alpha)-Isomer;Ethylmorphine Hydrochloride, Dihydrate, (5alpha,6alpha)-Isomer;Ethylmorphine Sulfate (2:1), (5alpha,6alpha)-Isomer;Ethylmorphine, (5alpha,6beta)-Isomer;Trachyl

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

Chemical Property of Ethylmorphine Edit

Chemical Property:

Vapor Pressure:1.01E-09mmHg at 25°C
Melting Point:40-42°C
Refractive Index:1.5000 (estimate)
Boiling Point:472.2 ºC at 760 mmHg
PKA:pKa 8.20(50% aq EtOH) (Uncertain)
Flash Point:239.4 ºC
PSA：41.93000
Density:1.31 g/cm³
LogP:1.82910
Storage Temp.:2-8°C
Water Solubility.:2.794g/L(20 oC)
XLogP3:1.5
Hydrogen Bond Donor Count:1
Hydrogen Bond Acceptor Count:4
Rotatable Bond Count:2
Exact Mass:313.16779360
Heavy Atom Count:23
Complexity:523

Purity/Quality:

Safty Information:

Pictogram(s): Xn
Hazard Codes:Xn,T,F
Statements: 22-39/23/24/25-23/24/25-11
Safety Statements: 36/37/39-45-36/37-16-7

MSDS Files:

SDS file from LookChem

Total 1 MSDS from other Authors

Useful:

Canonical SMILES:CCOC1=C2C3=C(CC4C5C3(CCN4C)C(O2)C(C=C5)O)C=C1
Isomeric SMILES:CCOC1=C2C3=C(C[C@@H]4[C@H]5[C@]3(CCN4C)[C@@H](O2)[C@H](C=C5)O)C=C1
Uses Ethyl Morphine, is an analgesic (narcotic), antitussive, and Mydriatic. Controlled substance. Analgesic (narcotic); antitussive. Mydriatic. Controlled substance.
Therapeutic Function Analgesic, Antitussive, Mydriatic

Technology Process of Ethylmorphine

There total 10 articles about Ethylmorphine 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: