Cas 97583-68-1,endo,endo-bis-N-phenylimide of 1,8-dimethylbicyclo<2.2.2>oct-7-ene-2,3,5,6-tetracarboxylic acid

97583-68-1

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Basic information

Product Name: endo,endo-bis-N-phenylimide of 1,8-dimethylbicyclo<2.2.2>oct-7-ene-2,3,5,6-tetracarboxylic acid
Synonyms:
CAS NO:97583-68-1
Molecular Formula:
Molecular Weight: 426.472
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,endo-bis-N-phenylimide of 1,8-dimethylbicyclo<2.2.2>oct-7-ene-2,3,5,6-tetracarboxylic acid(CAS DataBase Reference)
NIST Chemistry Reference: endo,endo-bis-N-phenylimide of 1,8-dimethylbicyclo<2.2.2>oct-7-ene-2,3,5,6-tetracarboxylic acid(97583-68-1)
EPA Substance Registry System: endo,endo-bis-N-phenylimide of 1,8-dimethylbicyclo<2.2.2>oct-7-ene-2,3,5,6-tetracarboxylic acid(97583-68-1)

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: 97583-68-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 97583-68-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 9,7,5,8 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 97583-68:
(7*9)+(6*7)+(5*5)+(4*8)+(3*3)+(2*6)+(1*8)=191
191 % 10 = 1
So 97583-68-1 is a valid CAS Registry Number.

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97583-68-1Relevant academic research and scientific papers

DIENE SYNTHESIS WITH 2-PYRONES AND 2-PYRIDONES. XXXIII. STEREOCHEMISTRY OF THE DOUBLE DIENE SYNTHESIS OF 2-PYRONES WITH N-PHENYLMALEIMIDE

Nesterova, T. L.,Shusherina, N. P.,Shulishov, E. V.

, p. 387 - 390 (2007/10/02)

The stereeochemistry of the successive addition of two molecules of N-phenylmaleimide to 2-pyrones was investigated for the first time.Irrespective of the structure, the reaction of the pyrones with N-phenylmaleimide takes place stereoselectively with the

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