Ethylmorphine hydrochloride

Base Information

• Chemical Name: Ethylmorphine hydrochloride
• CAS No.: 125-30-4
• Molecular Formula: C19H23 N O3 . Cl H
• Molecular Weight: 349.89
• European Community (EC) Number: 204-734-4
• UNII: MFM5450P3T
• DSSTox Substance ID: DTXSID70924986
• Wikidata: Q26840900
• NCI Thesaurus Code: C76842
• ChEMBL ID: CHEMBL2107695
• Mol file: 125-30-4.mol

Synonyms:ethylmorphine hydrochloride;Ethylmorphine HCl;CODETHYLINE HYDROCHLORIDE;125-30-4;O-Ethylmorphine hydrochloride;Dionin hydrochloride;Dionine hydrochloride;UNII-MFM5450P3T;MFM5450P3T;3-O-Ethylmorphine hydrochloride;EINECS 204-734-4;Ethylmorphine hydrochloride [JAN:NF];(4R,4aR,7S,7aR,12bS)-9-ethoxy-3-methyl-2,4,4a,7,7a,13-hexahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinolin-7-ol;hydrochloride;Ethylmorphine hydrochloride [JAN];SCHEMBL220710;CHEMBL2107695;DTXSID70924986;ETHYLMORPHINE HYDROCHLORIDE [WHO-DD];Morphinan-6-alpha-ol, 7,8-didehydro-4,5-alpha-epoxy-3-ethoxy-17-methyl-, hydrochloride;ETHYLMORPHINE HYDROCHLORIDE [EP MONOGRAPH];ETHYLMORPHINE HYDROCHLORIDE ANHYDROUS [MI];Q26840900;(5.ALPHA.,6.ALPHA.)-7,8-DIDEHYDRO-4,5-EPOXY-3-ETHOXY-17-METHYLMORPHINAN-6-OL HYDROCHLORIDE;Morphinan-6-ol, 7,8-didehydro-4,5-epoxy-3-ethoxy-17-methyl-, hydrochloride, (5.alpha.,6.alpha.)-

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

Chemical Property of Ethylmorphine hydrochloride

Chemical Property:

• Vapor Pressure: 1.01E-09mmHg at 25°C
• Boiling Point: 472.2°Cat760mmHg
• Flash Point: 239.4°C
• Density: 1.31g/cm³
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 2
• Exact Mass: 349.1444713
• Heavy Atom Count: 24
• Complexity: 523

Purity/Quality:

Safty Information:

• Pictogram(s): Toxic by ingestion; habit-forming narcotic.
• Hazard Codes: Toxic by ingestion; habit-forming narcotic.

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CCOC1=C2C3=C(CC4C5C3(CCN4C)C(O2)C(C=C5)O)C=C1.Cl
• 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.Cl