601494-86-4 Usage
Molecular Weight
262.28 g/mol
Structure
A seven-carbon cyclic compound with two carbonyl (C=O) functional groups and a 3,6-dioxoheptyl group attached to the 1st carbon.
Family
Pyrrolidinedione
Potential Applications
Pharmaceutical, polymer, and agrochemical industries due to its unique chemical structure and reactivity.
Additional Research
Further studies are needed to fully explore its potential uses and properties.
Check Digit Verification of cas no
The CAS Registry Mumber 601494-86-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,0,1,4,9 and 4 respectively; the second part has 2 digits, 8 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 601494-86:
(8*6)+(7*0)+(6*1)+(5*4)+(4*9)+(3*4)+(2*8)+(1*6)=144
144 % 10 = 4
So 601494-86-4 is a valid CAS Registry Number.
601494-86-4Relevant academic research and scientific papers
A convenient approach to the synthesis of 2-(2-aminoethyl)pyrroles and their heterocyclization into hydrogenated pyrrolopyridines and related pyrroloindolizines
Raiman, Marina V.,Pukin, Aleksei V.,Tyvorskii, Vladimir I.,De Kimpe, Norbert,Kulinkovich, Oleg G.
, p. 5265 - 5272 (2007/10/03)
2-(2-Aminoethyl)pyrroles and 2-(2-succinimidoethyl)pyrroles were prepared from acetals of ethyl 4-oxoalkanoates via latent vinyl 1,4-dicarbonyl compounds as the key intermediates. The Pictet-Spengler condensation of 2-(2-aminoethyl)pyrroles with aromatic aldehydes gave 4,5,6,7-tetrahydro-1H-pyrrolo[3,2-c]pyridines in good yields. 4,5,7,8,9,9a-Hexahydro-3H-pyrrolo[2,3-g]indolizines were prepared in a similar way starting from 2-(2-succinimidoethyl)pyrroles.
