Cas 1306623-65-3,(2S,12bS,Z)-3-(1-hydroxyethylidene)-2-(4-nitrophenyl)-1,2,3,6,7,12b-hexahydroindolo[2,3-a]quinolizin-4(12H)-one

1306623-65-3

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Basic information

Product Name: (2S,12bS,Z)-3-(1-hydroxyethylidene)-2-(4-nitrophenyl)-1,2,3,6,7,12b-hexahydroindolo[2,3-a]quinolizin-4(12H)-one
Synonyms: (2S,12bS,Z)-3-(1-hydroxyethylidene)-2-(4-nitrophenyl)-1,2,3,6,7,12b-hexahydroindolo[2,3-a]quinolizin-4(12H)-one
CAS NO:1306623-65-3
Molecular Formula:
Molecular Weight: 403.437
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: (2S,12bS,Z)-3-(1-hydroxyethylidene)-2-(4-nitrophenyl)-1,2,3,6,7,12b-hexahydroindolo[2,3-a]quinolizin-4(12H)-one(CAS DataBase Reference)
NIST Chemistry Reference: (2S,12bS,Z)-3-(1-hydroxyethylidene)-2-(4-nitrophenyl)-1,2,3,6,7,12b-hexahydroindolo[2,3-a]quinolizin-4(12H)-one(1306623-65-3)
EPA Substance Registry System: (2S,12bS,Z)-3-(1-hydroxyethylidene)-2-(4-nitrophenyl)-1,2,3,6,7,12b-hexahydroindolo[2,3-a]quinolizin-4(12H)-one(1306623-65-3)

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: 1306623-65-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1306623-65-3 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,3,0,6,6,2 and 3 respectively; the second part has 2 digits, 6 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 1306623-65:
(9*1)+(8*3)+(7*0)+(6*6)+(5*6)+(4*2)+(3*3)+(2*6)+(1*5)=133
133 % 10 = 3
So 1306623-65-3 is a valid CAS Registry Number.

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1306623-65-3Relevant academic research and scientific papers

Enantioselective organocatalyzed cascade reactions to highly functionalized quinolizidines

Dai, Xiaoyang,Wu, Xiaoyu,Fang, Huihui,Nie, Linlin,Chen, Jie,Deng, Hongmei,Cao, Weiguo,Zhao, Gang

experimental part, p. 3034 - 3040 (2011/05/14)

An organocatalyzed one-pot Michael addition-Pictet-Spengler sequence of β-ketoamides and α,β-unsaturated aldehydes was developed, which provided access to highly substituted indolo[2,3-α]quinolizidines and benzo[α]quinolizidines in moderate to good yields

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