Cas 933775-85-0,endo-3,5-dioxo-4-phenyl-4,10-diazatricyclo[5.2.1.0<sup>2,6</sup>]dec-8-ene-10-carboxylic acid methyl ester

933775-85-0

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Basic information

Product Name: endo-3,5-dioxo-4-phenyl-4,10-diazatricyclo[5.2.1.0^2,6]dec-8-ene-10-carboxylic acid methyl ester
Synonyms: endo-3,5-dioxo-4-phenyl-4,10-diazatricyclo[5.2.1.0^2,6]dec-8-ene-10-carboxylic acid methyl ester
CAS NO:933775-85-0
Molecular Formula:
Molecular Weight: 298.298
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: endo-3,5-dioxo-4-phenyl-4,10-diazatricyclo[5.2.1.0^2,6]dec-8-ene-10-carboxylic acid methyl ester(CAS DataBase Reference)
NIST Chemistry Reference: endo-3,5-dioxo-4-phenyl-4,10-diazatricyclo[5.2.1.0^2,6]dec-8-ene-10-carboxylic acid methyl ester(933775-85-0)
EPA Substance Registry System: endo-3,5-dioxo-4-phenyl-4,10-diazatricyclo[5.2.1.0^2,6]dec-8-ene-10-carboxylic acid methyl ester(933775-85-0)

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: 933775-85-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 933775-85-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 9,3,3,7,7 and 5 respectively; the second part has 2 digits, 8 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 933775-85:
(8*9)+(7*3)+(6*3)+(5*7)+(4*7)+(3*5)+(2*8)+(1*5)=210
210 % 10 = 0
So 933775-85-0 is a valid CAS Registry Number.

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933775-85-0Relevant academic research and scientific papers

Epibatidine alkaloid chemistry: 5. Domino-heck reactions of azabicyclic and tricyclic systems

Yolacan, Cigdem,Bagdatli, Emine,Oecal, Nueket,Kaufmann, Dieter E.

, p. 603 - 614 (2006)

Palladium-catalyzed hydroarylations and additional domino reactions of azabicyclic and tricyclic norbornene derivatives were investigated and a series of new epibatidine analogues were synthesized.

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