Hasubanan

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Column 1	Column 2
IUPAC name
(3aS-cis)-2,3,4,5-Tetrahydro-3a,9b-butano-1H-benz[e]indole
CAS Number	.mw-parser-output .plainlist ol,.mw-parser-output .plainlist ul{line-height:inherit;list-style:none;margin:0;padding:0}.mw-parser-output .plainlist ol li,.mw-parser-output .plainlist ul li{margin-bottom:0}14510-67-9 Y
3D model (JSmol)	Interactive image
ChEBI	CHEBI:35647 Y
ChemSpider	20152973 Y
PubChem CID	6857499
UNII	8K38RGP7SY Y
CompTox Dashboard (EPA)	DTXSID60425891
InChI
InChI=1S/C16H21N/c1-2-6-14-13(5-1)7-10-16-9-4-3-8-15(14,16)11-12-17-16/h1-2,5-6,17H,3-4,7-12H2/t15-,16+/m1/s1 YKey: RKWPQIQYRNOTMT-CVEARBPZSA-N YInChI=1/C16H21N/c1-2-6-14-13(5-1)7-10-16-9-4-3-8-15(14,16)11-12-17-16/h1-2,5-6,17H,3-4,7-12H2/t15-,16+/m1/s1Key: RKWPQIQYRNOTMT-CVEARBPZBP
SMILES
C2C[C@]14CCCC[C@@]4(CCN1)c3ccccc23
Chemical formula	C16H21N
Molar mass	227.351 g·mol−1
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
Y verify (what is YN ?)

Infobox references | |

Hasubanan is an alkaloid with the chemical formula of C16H21N. It forms the central core of a class of alkaloids known collectively as hasubanans. The compound is derived from reticuline, as is morphinan, but is comparatively more oxidized and rearranged. It is similar to acutumine.

Various alkaloids of this family have been synthesized in the laboratories.

• Hasubanonine

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• Synthesis at chem.wisc.edu

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