Cas 89240-54-0,(1S,12bR)-12-Benzyl-1-ethyl-1,4,6,7,12,12b-hexahydro-indolo[2,3-a]quinolizine-1-carbonitrile

89240-54-0

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Basic information

Product Name: (1S,12bR)-12-Benzyl-1-ethyl-1,4,6,7,12,12b-hexahydro-indolo[2,3-a]quinolizine-1-carbonitrile
Synonyms: (1S,12bR)-12-Benzyl-1-ethyl-1,4,6,7,12,12b-hexahydro-indolo[2,3-a]quinolizine-1-carbonitrile
CAS NO:89240-54-0
Molecular Formula:
Molecular Weight: 367.494
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: (1S,12bR)-12-Benzyl-1-ethyl-1,4,6,7,12,12b-hexahydro-indolo[2,3-a]quinolizine-1-carbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: (1S,12bR)-12-Benzyl-1-ethyl-1,4,6,7,12,12b-hexahydro-indolo[2,3-a]quinolizine-1-carbonitrile(89240-54-0)
EPA Substance Registry System: (1S,12bR)-12-Benzyl-1-ethyl-1,4,6,7,12,12b-hexahydro-indolo[2,3-a]quinolizine-1-carbonitrile(89240-54-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 89240-54-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 89240-54-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,9,2,4 and 0 respectively; the second part has 2 digits, 5 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 89240-54:
(7*8)+(6*9)+(5*2)+(4*4)+(3*0)+(2*5)+(1*4)=150
150 % 10 = 0
So 89240-54-0 is a valid CAS Registry Number.

89240-54-0Upstream product

89240-54-0Downstream Products

89240-55-1 (1S,12bR)-12-Benzyl-1-ethyl-1,2,3,4,6,7,12,12b-octahydro-indolo[2,3-a]quinolizine-1-carbonitrile

89240-54-0Relevant academic research and scientific papers

New approaches to the synthesis of eburnane alkaloids

Langlois,Pouilhes,Genin,et al.

, p. 3755 - 3761 (1983)

The aldehyde which is a key precursor of the Eburnane alkaloid vincamine has been prepared in two ways. The first one involves a photochemical rearrangement of a spiro oxaziridine intermediate and the second is based on an imino Diels-Alder reaction follo

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