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Technology Process of (1aR,5aR,13S,13aS)-13-Ethyl-4,5,11,12,13,13a-hexahydro-2H-3,13-methanooxireno[9,10]azacycloundecino[5,4-b]indol-5a(1aH)-ol

(1aR,5aR,13S,13aS)-13-Ethyl-4,5,11,12,13,13a-hexahydro-2H-3,13-methanooxireno[9,10]azacycloundecino[5,4-b]indol-5a(1aH)-ol

Base Information
  • Chemical Name:(1aR,5aR,13S,13aS)-13-Ethyl-4,5,11,12,13,13a-hexahydro-2H-3,13-methanooxireno[9,10]azacycloundecino[5,4-b]indol-5a(1aH)-ol
  • CAS No.:18269-16-4
  • Molecular Formula:C19H24N2O2
  • Molecular Weight:312.4061
  • Hs Code.:
(1aR,5aR,13S,13aS)-13-Ethyl-4,5,11,12,13,13a-hexahydro-2H-3,13-methanooxireno[9,10]azacycloundecino[5,4-b]indol-5a(1aH)-ol

Synonyms:voaphylline hydroxyindolenine;

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Chemical Property of (1aR,5aR,13S,13aS)-13-Ethyl-4,5,11,12,13,13a-hexahydro-2H-3,13-methanooxireno[9,10]azacycloundecino[5,4-b]indol-5a(1aH)-ol
Chemical Property:
  • Vapor Pressure:5.64E-10mmHg at 25°C 
  • Boiling Point:478.8°Cat760mmHg 
  • Flash Point:243.4°C 
  • PSA：48.36000 
  • Density:1.38g/cm3 
  • LogP:1.99710 
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SDS file from LookChem

Useful:
  • Description This alkaloid from the leaf extract of Voacanga africana has the above structure in neutral or basic media as determined by spectral data, particularly the mass spectra. In acid solution it exists as the quaternary base. Reduction with KBH4 yields Voaphylline (q.v.) and conversely the base may be formed from the latter by oxidation with peracetic acid.
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