Oxilorphan

Base Information

Chemical Name:Oxilorphan
CAS No.:42281-59-4
Molecular Formula:C20H27 N O2
Molecular Weight:313.44
Hs Code.:
European Community (EC) Number:255-749-8
UNII:9Y9J2J74TO
DSSTox Substance ID:DTXSID001009897
Wikipedia:Oxilorphan
Wikidata:Q7115662
NCI Thesaurus Code:C174594
ChEMBL ID:CHEMBL2106993
Mol file:42281-59-4.mol

Synonyms:L-N-cyclopropylmethyl-3,14-dihydroxymorphinan;oxilorphan;oxilorphan hydrochloride;oxilorphan hydrochloride, (+-)-isomer;oxilorphan hydrochloride, (9alpha,13alpha,14alpha)-isomer;oxilorphan tartrate (2:1), (R-(R*,R*))-isomer;oxilorphan tartrate, (R-(R*,R*))-isomer;oxilorphan, (+-)-isomer;oxilorphan, (14alpha)-(+-)-isomer;oxilorphan, (14alpha)-isomer

Suppliers and Price of Oxilorphan

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

American Custom Chemicals Corporation
OXILORPHAN 95.00%
5MG
$ 497.83

Total 0 raw suppliers

Chemical Property of Oxilorphan

Chemical Property:

Vapor Pressure:1.24E-10mmHg at 25°C
Melting Point:174°C
Refractive Index:1.5614 (estimate)
Boiling Point:495.4°Cat760mmHg
PKA:10.06±0.40(Predicted)
Flash Point:262.9°C
PSA：43.70000
Density:1.27g/cm³
LogP:2.91340
XLogP3:3.2
Hydrogen Bond Donor Count:2
Hydrogen Bond Acceptor Count:3
Rotatable Bond Count:2
Exact Mass:313.204179104
Heavy Atom Count:23
Complexity:478

Purity/Quality:: OXILORPHAN 95.00% ^*data from reagent suppliers

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Canonical SMILES:C1CCC2(C3CC4=C(C2(C1)CCN3CC5CC5)C=C(C=C4)O)O
Isomeric SMILES:C1CC[C@]2([C@H]3CC4=C([C@]2(C1)CCN3CC5CC5)C=C(C=C4)O)O
Uses Antagonist (to narcotics).

Technology Process of Oxilorphan

There total 7 articles about Oxilorphan 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:

: 67-56-1
methanol

: 1336-21-6
ammonium hydroxide

: 63708-59-8
7-Methoxy-2-oxo-1,2,3,4-tetrahydro-1-naphthalene acetonitrile

: 42281-59-4
N-cyclopropylmethyl-3,14β-dihydroxymorphinan

Guidance literature:: With boron tribromide; In dichloromethane; water;

Reference yield:

: 4133-34-0
7-methoxyl-2-tetralone

: 42281-59-4
N-cyclopropylmethyl-3,14β-dihydroxymorphinan

Guidance literature:: Multi-step reaction with 2 steps

1: water; benzene

2: boron tribromide / dichloromethane; water

With boron tribromide; In dichloromethane; water; benzene;