Cas 114133-18-5,4-<(carbaniloyloxy)methyl>-7-(benzoyloxy)-3a,4,7,7a-tetrahydro-2-phenyl-1,3-isoindoledione

114133-18-5

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Basic information

Product Name: 4-<(carbaniloyloxy)methyl>-7-(benzoyloxy)-3a,4,7,7a-tetrahydro-2-phenyl-1,3-isoindoledione
Synonyms: 4-<(carbaniloyloxy)methyl>-7-(benzoyloxy)-3a,4,7,7a-tetrahydro-2-phenyl-1,3-isoindoledione
CAS NO:114133-18-5
Molecular Formula:
Molecular Weight: 496.519
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: 4-<(carbaniloyloxy)methyl>-7-(benzoyloxy)-3a,4,7,7a-tetrahydro-2-phenyl-1,3-isoindoledione(CAS DataBase Reference)
NIST Chemistry Reference: 4-<(carbaniloyloxy)methyl>-7-(benzoyloxy)-3a,4,7,7a-tetrahydro-2-phenyl-1,3-isoindoledione(114133-18-5)
EPA Substance Registry System: 4-<(carbaniloyloxy)methyl>-7-(benzoyloxy)-3a,4,7,7a-tetrahydro-2-phenyl-1,3-isoindoledione(114133-18-5)

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: 114133-18-5(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 114133-18-5 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,4,1,3 and 3 respectively; the second part has 2 digits, 1 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 114133-18:
(8*1)+(7*1)+(6*4)+(5*1)+(4*3)+(3*3)+(2*1)+(1*8)=75
75 % 10 = 5
So 114133-18-5 is a valid CAS Registry Number.

114133-18-5Upstream product

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114133-18-5Relevant academic research and scientific papers

Intra- and Intermolecular Diels-Alder Reactions of Glutaconaldehyde Derivatives

Becher, Jan,Nielsen, Helle Chris,Jacobsen, Jens Peter,Simonsen, Ole,Clausen, Helen

, p. 1862 - 1871 (2007/10/02)

The intramolecular Diels-Alder reaction of the alcohols 10a-d and maleic anhydride gave the cis-fused cycloadducts 12a-d, whereas the esters 13a and 13c prepared from 10a and fumaric acid ethyl or methyl ester monochloride produced trans-fused adducts 14a

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