Cas 118355-91-2,(1S,2aS,4aS,9bR)-2a-Benzoyl-1,2,2a,3,4,4a,5,9b-octahydro-pyrrolizino[3,4,5-ab]isoquinoline-1,3-dicarbonitrile

118355-91-2

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Basic information

Product Name: (1S,2aS,4aS,9bR)-2a-Benzoyl-1,2,2a,3,4,4a,5,9b-octahydro-pyrrolizino[3,4,5-ab]isoquinoline-1,3-dicarbonitrile
Synonyms:
CAS NO:118355-91-2
Molecular Formula:
Molecular Weight: 353.423
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,2aS,4aS,9bR)-2a-Benzoyl-1,2,2a,3,4,4a,5,9b-octahydro-pyrrolizino[3,4,5-ab]isoquinoline-1,3-dicarbonitrile(CAS DataBase Reference)
NIST Chemistry Reference: (1S,2aS,4aS,9bR)-2a-Benzoyl-1,2,2a,3,4,4a,5,9b-octahydro-pyrrolizino[3,4,5-ab]isoquinoline-1,3-dicarbonitrile(118355-91-2)
EPA Substance Registry System: (1S,2aS,4aS,9bR)-2a-Benzoyl-1,2,2a,3,4,4a,5,9b-octahydro-pyrrolizino[3,4,5-ab]isoquinoline-1,3-dicarbonitrile(118355-91-2)

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: 118355-91-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 118355-91-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,8,3,5 and 5 respectively; the second part has 2 digits, 9 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 118355-91:
(8*1)+(7*1)+(6*8)+(5*3)+(4*5)+(3*5)+(2*9)+(1*1)=132
132 % 10 = 2
So 118355-91-2 is a valid CAS Registry Number.

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118355-91-2Relevant academic research and scientific papers

Tandem 1,3-Dipolar Cycloadditions of Pyridinium or Isoquinolinium Methylides with Olefinic Dipolarophiles Leading to Cyclazines. "Enamine Route" as a New Generation Method of Azomethine Ylides

Kanemasa, Shuji,Takenaka, Shigeori,Watanabe, Haruyuki,Tsuge, Otohiko

, p. 420 - 424 (2007/10/02)

Pyridinium or isoquinolinium methylides undergo tandem 1,3-dipolar cycloadditions with two molecules of olefins to produce cyclazine derivatives in a highly regioselective, stereoselective, and face-selective manner.A new generation of azomethine y

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