Cas 53502-79-7,N-phenylimide of 2,3-dichlorobicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid

53502-79-7

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Basic information

Product Name: N-phenylimide of 2,3-dichlorobicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid
Synonyms: N-phenylimide of 2,3-dichlorobicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid
CAS NO:53502-79-7
Molecular Formula:
Molecular Weight: 308.164
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-phenylimide of 2,3-dichlorobicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid(CAS DataBase Reference)
NIST Chemistry Reference: N-phenylimide of 2,3-dichlorobicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid(53502-79-7)
EPA Substance Registry System: N-phenylimide of 2,3-dichlorobicyclo[2.2.1]hept-5-ene-2,3-dicarboxylic acid(53502-79-7)

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: 53502-79-7(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 53502-79-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,3,5,0 and 2 respectively; the second part has 2 digits, 7 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 53502-79:
(7*5)+(6*3)+(5*5)+(4*0)+(3*2)+(2*7)+(1*9)=107
107 % 10 = 7
So 53502-79-7 is a valid CAS Registry Number.

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53502-79-7Relevant academic research and scientific papers

REACTIVITY OF N-ARYL DICHLOROMALEINIMIDES IN DIENE SYNTHESIS REACTIONS WITH CYCLOPENTADIENE AND 1,3-CYCLOHEXADIENE

Nagiev, Ya. M.,Samuilova, Ya. D.,Bagirov, Sh. T.,Shnulin, A. N.,Adigezalov, V. A.,et al.

, p. 1309 - 1312 (2007/10/02)

The relative activity of 1,3-cyclohexadiene and cyclopentadiene in reactions with N-aryl dichloromaleinimides is to a large extent determined by differences in the 1,4-distance of the dienic systems.The reactions studied proceed according to the "diene-do

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