Cas 81246-04-0,N-(methoxycarbonyl)-3-endo-phenyl-2-azabicyclo<2.2.2>octane-5,6-endo-dicarboxylic anhydride

81246-04-0

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Basic information

Product Name: N-(methoxycarbonyl)-3-endo-phenyl-2-azabicyclo<2.2.2>octane-5,6-endo-dicarboxylic anhydride
Synonyms: N-(methoxycarbonyl)-3-endo-phenyl-2-azabicyclo<2.2.2>octane-5,6-endo-dicarboxylic anhydride
CAS NO:81246-04-0
Molecular Formula:
Molecular Weight: 315.326
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: N-(methoxycarbonyl)-3-endo-phenyl-2-azabicyclo<2.2.2>octane-5,6-endo-dicarboxylic anhydride(CAS DataBase Reference)
NIST Chemistry Reference: N-(methoxycarbonyl)-3-endo-phenyl-2-azabicyclo<2.2.2>octane-5,6-endo-dicarboxylic anhydride(81246-04-0)
EPA Substance Registry System: N-(methoxycarbonyl)-3-endo-phenyl-2-azabicyclo<2.2.2>octane-5,6-endo-dicarboxylic anhydride(81246-04-0)

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: 81246-04-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 81246-04-0 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,1,2,4 and 6 respectively; the second part has 2 digits, 0 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 81246-04:
(7*8)+(6*1)+(5*2)+(4*4)+(3*6)+(2*0)+(1*4)=110
110 % 10 = 0
So 81246-04-0 is a valid CAS Registry Number.

81246-04-0Upstream product

81246-04-0Downstream Products

40985-89-5 N-(methoxycarbonyl)-3-exo-phenyl-2-azabicyclo<2.2.2>oct-5-ene

81246-04-0Relevant academic research and scientific papers

Reexamination of Stereochemical Issues Concerning 2-Phenyl-1,2-dihydropyridine-Maleimide Cycloadditions

Krow, Grant R.,Carey, James T.,Zacharias, David E.,Knaus, Edward E.

, p. 1989 - 1993 (2007/10/02)

The reaction of N-acetyl- and N-(carbomethoxy)-2-phenyl-1,2-dihydropyridines 1d-e with maleimides 5a-c has been shown by chemical correlation and X-ray analysis to proceed with only endo-maleimide, anti-phenyl stereoselectivity, rather than via stereosele

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