Cas 83048-83-3,{(E)-[1-(4-Nitro-phenyl)-2,5-dioxo-pyrrolidin-3-yl]-phenyl-methylimino}-phenyl-acetonitrile

83048-83-3

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Basic information

Product Name: {(E)-[1-(4-Nitro-phenyl)-2,5-dioxo-pyrrolidin-3-yl]-phenyl-methylimino}-phenyl-acetonitrile
Synonyms:
CAS NO:83048-83-3
Molecular Formula:
Molecular Weight: 438.442
EINECS: N/A
Product Categories: N/A
Mol File: 83048-83-3.mol
Article Data: 1

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: {(E)-[1-(4-Nitro-phenyl)-2,5-dioxo-pyrrolidin-3-yl]-phenyl-methylimino}-phenyl-acetonitrile(CAS DataBase Reference)
NIST Chemistry Reference: {(E)-[1-(4-Nitro-phenyl)-2,5-dioxo-pyrrolidin-3-yl]-phenyl-methylimino}-phenyl-acetonitrile(83048-83-3)
EPA Substance Registry System: {(E)-[1-(4-Nitro-phenyl)-2,5-dioxo-pyrrolidin-3-yl]-phenyl-methylimino}-phenyl-acetonitrile(83048-83-3)

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: 83048-83-3(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 83048-83-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,3,0,4 and 8 respectively; the second part has 2 digits, 8 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 83048-83:
(7*8)+(6*3)+(5*0)+(4*4)+(3*8)+(2*8)+(1*3)=133
133 % 10 = 3
So 83048-83-3 is a valid CAS Registry Number.

83048-83-3Upstream product

83048-83-3Downstream Products

83048-83-3Relevant articles and documents

Stereoselectivity of Cycloaddition of N-(Cyanomethyl)- and N-(α-Cyanobenzyl)imines with Olefinic Dipolarophiles. Synthetic Equivalents of Nitrile Ylide 1,3-Dipoles

Tsuge, Otohiko,Ueno, Kazunori,Kanemasa, Shuji,Yorozu, Kiyotaka

, p. 1809 - 1824 (1986)

N-(Cyanomethyl)- and N-(α-cyanobenzyl)imines derived from a variety of aldehydes and ketones can tautomerize into N-protonated azomethine ylides which undergo cycloadditions with olefinic dipolarophiles.These cycloadditions are often accompanied by the el

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