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(2S)-1,2,3,4,4aβ,5,6,7,7a,12bβ-Decahydro-4α-(1-hydroxyethyl)-9-methoxy-2α,5α-methanoindolo[3,2-d][1]benzazepin-7a-ol

Base Information
  • Chemical Name:(2S)-1,2,3,4,4aβ,5,6,7,7a,12bβ-Decahydro-4α-(1-hydroxyethyl)-9-methoxy-2α,5α-methanoindolo[3,2-d][1]benzazepin-7a-ol
  • CAS No.:23627-68-1
  • Molecular Formula:C20H26N2O3
  • Molecular Weight:342.438
  • Hs Code.:
(2S)-1,2,3,4,4aβ,5,6,7,7a,12bβ-Decahydro-4α-(1-hydroxyethyl)-9-methoxy-2α,5α-methanoindolo[3,2-d][1]benzazepin-7a-ol

Synonyms:Iboxygainehydroxyindolenine (8CI); 6,9-Methano-5H-pyrido[1',2':1,2]azepino[4,5-b]indole,ibogamine-9,20(17H)-diol deriv.

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Chemical Property of (2S)-1,2,3,4,4aβ,5,6,7,7a,12bβ-Decahydro-4α-(1-hydroxyethyl)-9-methoxy-2α,5α-methanoindolo[3,2-d][1]benzazepin-7a-ol
Chemical Property:
  • Vapor Pressure:4.2E-12mmHg at 25°C 
  • Melting Point:271-2°C (dec.). 
  • Boiling Point:530.9°Cat760mmHg 
  • Flash Point:274.9°C 
  • PSA:65.29000 
  • Density:1.47g/cm3 
  • LogP:1.45350 
Purity/Quality:
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MSDS Files:

SDS file from LookChem

Useful:
  • Description A strychnine type alkaloid, this base is found in the leaves of Strychnos icaja Baill. It may be crystallized from MeOH when it yields colourless prisms. The alkaloid has [α]D - 10° (c 1.0, CHCI3) and the ultraviolet spectrum in EtOH shows absorption maxima at 254 and 291 mil. The structure has been established as that of N-methyl-sec-pseudostrychnine.
Technology Process of (2S)-1,2,3,4,4aβ,5,6,7,7a,12bβ-Decahydro-4α-(1-hydroxyethyl)-9-methoxy-2α,5α-methanoindolo[3,2-d][1]benzazepin-7a-ol

There total 1 articles about (2S)-1,2,3,4,4aβ,5,6,7,7a,12bβ-Decahydro-4α-(1-hydroxyethyl)-9-methoxy-2α,5α-methanoindolo[3,2-d][1]benzazepin-7a-ol 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:
Guidance literature:
Iboxygain, CHCl3 (Luftox.);
DOI:10.1021/jo01254a033
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