140424-48-2 Usage
Molecular structure
1H-Pyrrole-3-carboxylic acid, 2-(4-bromophenyl)-2,5-dihydro-4-hydroxy-1-(4-methylphenyl)-5-oxo-, 1,1-dimethylethyl ester consists of a pyrrole ring with a carboxylic acid functional group, a hydroxy group, and a ketone group attached to a phenyl ring. It also has a 4-bromophenyl group and a 4-methylphenyl group, both substituted on the pyrrole ring, and a 1,1-dimethylethyl ester functional group.
Functional groups
The compound contains several functional groups, including a carboxylic acid group, a hydroxy group, a ketone group, and an ester group (1,1-dimethylethyl ester).
Aromaticity
The compound has aromatic character due to the presence of the pyrrole and phenyl rings.
Substitution patterns
The 4-bromophenyl and 4-methylphenyl groups are substituted on the pyrrole ring, which may affect the compound's reactivity and properties.
Potential applications
This chemical compound may have applications in pharmaceuticals, materials science, or other fields due to its unique structure and properties.
Further research
More research and analysis are needed to fully understand and utilize the properties and potential applications of 1H-Pyrrole-3-carboxylic acid,
2-(4-bromophenyl)-2,5-dihydro-4-hydroxy-1-(4-methylphenyl)-5-oxo-,
1,1-dimethylethyl ester.
Check Digit Verification of cas no
The CAS Registry Mumber 140424-48-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,0,4,2 and 4 respectively; the second part has 2 digits, 4 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 140424-48:
(8*1)+(7*4)+(6*0)+(5*4)+(4*2)+(3*4)+(2*4)+(1*8)=92
92 % 10 = 2
So 140424-48-2 is a valid CAS Registry Number.
140424-48-2Relevant academic research and scientific papers
FIVE-MEMBERED 2,3-DIOXOHETEROCYCLES. XXI. SYNTHESIS OF 1,5-DIARYL-4-TERT-BUTOXYCARBONYL-3-HYDROXY-2,5-DIHYDRO-2-PYRROLONES AND THEIR REACTION WITH ARYLAMINES AND o-PHENYLENEDIAMINE
Gein, V. L.,Voronina, E. V.,Andreichikov, Yu. S.
, p. 1722 - 1729 (2007/10/02)
The reaction of di-tert-butyl oxaloacetate or its potassium salt with Schiff bases gave 1,5-diaryl-4-tert-butoxycarbonyl-3-hydroxy-2,5-dihydro-2-pyrrolones.Reaction of the latter with arylamines led to N-aryl-1,5-diaryl-3-hydroxy-2-oxo-4-pyrrolecarboxamides.The reaction with o-phenylenediamine gave 2,3-diaryl-1,4-dioxo-5H,10H-1,3-dihydropyrrolo-1,5-benzodiazepines.
