Morphine methylbromide

Base Information

• Chemical Name: Morphine methylbromide
• CAS No.: 125-23-5
• Molecular Formula: Br*C₁₈H₂₂NO₃
• Molecular Weight: 380.282
• UNII: 1A51P5NGGU
• DSSTox Substance ID: DTXSID90924983
• Wikipedia: Morphine_methylbromide
• Wikidata: Q6913412
• Mol file: 125-23-5.mol

Synonyms:MORPHINE METHYLBROMIDE;Morphosan;Morphine bromomethylate;DEA No. 9305;125-23-5;UNII-1A51P5NGGU;1A51P5NGGU;7,8-Didehydro-4,5-alpha-epoxy-3,6-alpha-dihydroxy-17,17-dimethylmorphinanium bromide;Morphinanium, 7,8-didehydro-3,6-alpha-dihydroxy-17,17-dimethyl-4,5-alpha-epoxy-, bromide;(4R,4aR,7S,7aR,12bS)-3,3-dimethyl-2,4,4a,7,7a,13-hexahydro-1H-4,12-methanobenzofuro[3,2-e]isoquinolin-3-ium-7,9-diol;bromide;morphine methobromide;IDS-NM-009METH;C18H22NO3.Br;C18-H22-N-O3.Br;DTXSID90924983;MORPHINE METHYLBROMIDE [WHO-DD];LS-91828;Q6913412;MORPHINANIUM, 7,8-DIDEHYDRO-4,5-EPOXY-3,6-DIHYDROXY-17,17-DIMETHYL-, BROMIDE (1:1), (5.ALPHA.,6.ALPHA.)-;MORPHINANIUM, 7,8-DIDEHYDRO-4,5-EPOXY-3,6-DIHYDROXY-17,17-DIMETHYL-, BROMIDE, (5.ALPHA.,6.ALPHA.)-

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Chemical Property of Morphine methylbromide

Chemical Property:

• PSA: 52.52000
• LogP: 2.69780
• Hydrogen Bond Donor Count: 2
• Hydrogen Bond Acceptor Count: 4
• Rotatable Bond Count: 0
• Exact Mass: 379.07831
• Heavy Atom Count: 23
• Complexity: 532

Purity/Quality:

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: C[N+]1(CCC23C4C1CC5=C2C(=C(C=C5)O)OC3C(C=C4)O)C.[Br-]
• Isomeric SMILES: C[N+]1(CC[C@]23[C@@H]4[C@H]1CC5=C2C(=C(C=C5)O)O[C@H]3[C@H](C=C4)O)C.[Br-]
• Uses: Morphosan is a derivative of the opioid morphine (CAS# 57-27-2).

Technology Process of Morphine methylbromide

There total 1 articles about Morphine methylbromide 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:

methyl bromide (74-83-9) + MORPHIN (57-27-2) → 4,5α-epoxy-3,6α-dihydroxy-17,17-dimethyl-morphin-7-enium; bromide (125-23-5)

Guidance literature:

With ethanol;

upstream raw materials:

methyl bromide

MORPHIN