4874-57-1 Usage
Carboxamide derivative
It is a derivative of a carboxamide, which is a functional group consisting of an amide group (-CONH2) attached to an alkyl or aryl group.
Cyclopentene ring
The compound contains a five-membered carbon ring with a double bond between two of the carbon atoms.
Phenyl group
A phenyl group, which is a six-membered carbon ring with alternating single and double bonds, is attached to the cyclopentene ring.
Organic synthesis and pharmaceutical research
The compound is used as a building block in the creation of new chemical compounds, particularly in the fields of organic synthesis and pharmaceutical research.
Potential applications in drug development and medical treatments
Although further research is needed, this compound may have potential applications in the development of new drugs and other medical treatments due to its unique structure and properties.
Need for further research
A deeper understanding of the properties and potential uses of 1-Cyclopentene-1-carboxamide, N-phenyl-2-(phenylamino)is required to fully explore its applications in various fields.
Check Digit Verification of cas no
The CAS Registry Mumber 4874-57-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,7 and 4 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 4874-57:
(6*4)+(5*8)+(4*7)+(3*4)+(2*5)+(1*7)=121
121 % 10 = 1
So 4874-57-1 is a valid CAS Registry Number.
4874-57-1Relevant articles and documents
Redox Property of Enamines
Li, Yao,Wang, Dehong,Zhang, Long,Luo, Sanzhong
, p. 12071 - 12090 (2019/10/11)
Enamines are electron-rich compounds bearing intriguing redox properties. Herein, a series of secondary enamines condensed from primary amine and β-ketocarbonyls were synthesized and their electrochemical oxidation properties were systematically studied by cyclic voltammetry. Furthermore, theoretical calculation of oxidation potentials of enamines, particularly those catalytic intermediates, was also conducted to further broaden the scope investigated. Possible structural factors on oxidation and the nature of the resulted radical cation intermediates were revealed and discussed. Correlation of redox potentials with molecular properties such as highest occupied molecular orbital energies and natural population analysis charge were explored, and there appears no simple linear correlation. On the other hand, a good correlation with Mayr's nucleophilicity parameter N was noted among a range of catalytically relevant enamines. Spin population analysis disclosed that enamine radical cations mainly exhibit the carbon-center free radical feature. Taking experimental and computation data together, a comprehensive picture about the redox property of enamines is presented, which would provide guidance in the development of oxidative enamine catalysis and transformations.
