142154-88-9 Usage
Pyrrole derivative
The compound is based on a pyrrole ring, which is a five-membered ring with one nitrogen atom.
Carbonitrile group
A cyano group (CN) is attached to the third position of the pyrrole ring, giving the compound its characteristic nitrile properties.
4-chlorophenyl group
A chlorine atom is attached to a phenyl ring (a six-membered carbon ring with delocalized pi electrons) at the 4th position of the pyrrole ring.
Trifluoromethyl group
Three fluorine atoms are attached to a methyl group (a carbon atom with three hydrogen atoms) at the 5th position of the pyrrole ring.
Research and industrial applications
The compound may be used in various applications, including the synthesis of pharmaceutical compounds and agrochemicals.
Biological activities
The compound may have potential biological activities and is of interest in medicinal chemistry and drug discovery.
Check Digit Verification of cas no
The CAS Registry Mumber 142154-88-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,2,1,5 and 4 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 142154-88:
(8*1)+(7*4)+(6*2)+(5*1)+(4*5)+(3*4)+(2*8)+(1*8)=109
109 % 10 = 9
So 142154-88-9 is a valid CAS Registry Number.
142154-88-9Relevant academic research and scientific papers
The Synthesis of Pyrroles with Insecticidal Activity
Kuhn, David G.,Kamhi, Victor M.,Furch, Joseph A.,Diehl, Robert E.,Lowen, Gregory T.,Kameswaran, Venkataraman
, p. 279 - 286 (2007/10/03)
The 2-aryl-4-bromo-5-trifluoromethylpyrrole-3-carbonitriles represent a new class of insect control agents. The high insecticidal activity observed in this series prompted us to investigate the preparation of regioisomeric arylhalotrifluoromethylpyrrole c
Process for the preparation of insecticidal, nematicidal and acaricidal 4-substituted-5-(trifluoromethyl)pyrrole-3-carbonitrile compounds
-
, (2008/06/13)
There is provided a process for the preparation of 4-substituted-5-(trifluoromethyl)pyrrole-3-carbonitrile compounds which are useful as insecticidal, nematicidal and acaricidal agents.
