144062-76-0 Usage
Pyrrole derivative
1H-Pyrrole-2-carbonitrile
A modification of the pyrrole structure, which is a five-membered aromatic ring with one nitrogen atom, by the addition of a carbonitrile group (C≡N).
Carbonitrile group
C≡N
A functional group consisting of a carbon-nitrogen triple bond, which imparts specific chemical properties to the compound.
Substituents
bromomethyl, phenyl, dichloro
Bromomethyl (CH2Br)
A methyl group (CH3) with one hydrogen atom replaced by a bromine atom (Br).
Phenyl
A benzene ring, a six-membered aromatic ring with delocalized electrons.
Dichloro (Cl2)
Two chlorine atoms (Cl) attached to the compound.
Potential applications
organic synthesis, pharmaceutical research
The compound may be useful in creating new organic compounds and could be relevant in the development of pharmaceuticals.
Biological activity
possible
The compound's structure suggests that it may interact with biological systems, potentially leading to new drug development.
Further studies and research needed
yes
More investigation is required to fully understand the compound's properties, uses, and potential applications.
Check Digit Verification of cas no
The CAS Registry Mumber 144062-76-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,4,0,6 and 2 respectively; the second part has 2 digits, 7 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 144062-76:
(8*1)+(7*4)+(6*4)+(5*0)+(4*6)+(3*2)+(2*7)+(1*6)=110
110 % 10 = 0
So 144062-76-0 is a valid CAS Registry Number.
144062-76-0Relevant articles and documents
Nonpeptide angiotensin II antagonists: N-phenyl-1H-pyrrole derivatives are angiotensin II receptor antagonists
Bovy,Reitz,Collins,Chamberlain,Olins,Corpus,McMahon,Palomo,Koepke,Smits,McGraw,Gaw
, p. 101 - 110 (2007/10/02)
A series of 5-[1-[4-[(4,5-disubstituted-1H-imidazol-1-yl)methyl]- substituted]-1H-pyrrol-2-yl]-1H-tetrazoles and 5-[1-[4-[(3,5-dibutyl-1H- 1,2,4-triazol-1-yl)methyl]-substituted]-1H-pyrrol-2-yl]-1H-tetrazoles were investigated as novel AT1-sele
