6-Dsmb-oxymorphone

Base Information

• Chemical Name: 6-Dsmb-oxymorphone
• CAS No.: 92398-22-6
• Molecular Formula: C₂₁H₂₃NO₅
• Molecular Weight: 369.417
• DSSTox Substance ID: DTXSID90919197
• Mol file: 92398-22-6.mol

Synonyms:4,5-epoxy-3,6,14-trihydroxy-6-(2-carboxyallyl)-17-methylmorphinan gamma-lactone;4,5-epoxy-3,6,14-trihydroxy-6-(2-carboxyallyl)-17-methylmorphinan gamma-lactone, (3,6beta,14-tri-OH)(6alpha-carboxy)-isomer;6-DSMB-oxymorphone

Chemical Property of 6-Dsmb-oxymorphone

Chemical Property:

• Boiling Point: 617.4°Cat760mmHg
• Flash Point: 327.2°C
• PSA: 79.23000
• Density: 1.48g/cm³
• LogP: 1.35590
• XLogP3: -0.1
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 6
• Rotatable Bond Count: 0
• Exact Mass: 369.15762283
• Heavy Atom Count: 27
• Complexity: 740

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CN1CCC23C4C5(CCC2(C1CC6=C3C(=C(C=C6)O)O4)O)CC(=C)C(=O)O5
• Isomeric SMILES: CN1CC[C@]23[C@@H]4C5(CC[C@]2([C@H]1CC6=C3C(=C(C=C6)O)O4)O)CC(=C)C(=O)O5

Technology Process of 6-Dsmb-oxymorphone

There total 1 articles about 6-Dsmb-oxymorphone 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:

4,5α-epoxy-3,6α,14-trihydroxy-6β-(2-carboxyallyl)-17-methylmorphinan γ-lactone 14-acetate ester (92398-23-7) → 4,5α-epoxy-3,6α,14-trihydroxy-6β-(2-carboxyallyl)-17-methylmorphinan γ-lactone (92398-22-6)

Guidance literature:

In methanol; at 45 ℃; for 14h;

DOI:10.1021/jm00378a032

upstream raw materials:

4,5α-epoxy-3,6α,14-trihydroxy-6β-(2-carboxyallyl)-17-methylmorphinan γ-lactone 14-acetate ester