675876-23-0 Usage
Pyrrole ring
A five-membered aromatic ring with four carbon atoms and one nitrogen atom, contributing to the compound's stability and aromaticity.
Acetamide group
A functional group consisting of an amide group (-CONH2) attached to a methyl group (-CH3), providing hydrogen bonding capabilities and polar character.
Sulfonyl group
A group containing a sulfur atom double-bonded to two oxygen atoms (-SO2), contributing to the compound's reactivity and polarity.
Propenyl group
A three-carbon chain with one double bond between two of the carbons (-CH=CH-CH3), allowing for addition reactions and further functionalization.
Phenylmethyl amino group
A phenyl ring (-C6H5) attached to an amino group (-NH2) via a methyl group (-CH3), providing opportunities for hydrogen bonding and potential pharmacological activity.
Nitrophenyl substituent
A phenyl ring (-C6H5) with a nitro group (-NO2) attached, which can influence the compound's reactivity, polarity, and potential applications.
These functional groups and structural features make 1H-Pyrrole-2-acetamide, 1-[(2-nitrophenyl)sulfonyl]-a-[(1-oxo-2-propenyl)(phenylmethyl)amino]-N-(phenylmethyl)a potentially versatile compound for various applications. However, further study and analysis are needed to determine its specific properties and uses.
Check Digit Verification of cas no
The CAS Registry Mumber 675876-23-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 6,7,5,8,7 and 6 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 675876-23:
(8*6)+(7*7)+(6*5)+(5*8)+(4*7)+(3*6)+(2*2)+(1*3)=220
220 % 10 = 0
So 675876-23-0 is a valid CAS Registry Number.
675876-23-0Relevant academic research and scientific papers
An Atom-Economical Approach to Conformationally Constrained Tricyclic Nitrogen Heterocycles via Sequential and Tandem Ugi/Intramolecular Diels-Alder Reaction of Pyrrole
Paulvannan
, p. 1207 - 1214 (2007/10/03)
An efficient approach to rigid tricyclic nitrogen heterocycles via sequential and tandem Ugi/intramolecular Diels-Alder (IMDA) cycloaddition of pyrrole is described. The one-pot Ugi four-component condensation (4CC) reaction was used as the key transforma
