143383-67-9 Usage
Molecular structure
A complex structure consisting of a quinoline ring system with various substituents.
Quinoline ring system
The core structure of the compound, which is a fused bicyclic compound with a nitrogen atom in the ring.
Fluoro substituent
A fluorine atom attached to the quinoline ring, which may influence the compound's pharmacological properties and reactivity.
Trifluoromethyl substituent
A carbon atom bonded to three fluorine atoms, attached to the quinoline ring, contributing to the compound's stability and potential applications in imaging or analytical chemistry.
Carboxylic acid group
A functional group (-COOH) present in the compound, which is responsible for its acidic properties and may be involved in hydrogen bonding and interactions with biological targets.
Pyrrolidinyl moiety
A five-membered nitrogen-containing ring attached to the quinoline core, which may contribute to the compound's pharmacological activity and potential as an antibiotic or antimicrobial agent.
Potential pharmacological properties
The compound may exhibit antibiotic or antimicrobial activity, making it of interest for drug development and medicinal chemistry research.
Unique structure
The compound's intricate and complex structure may make it a valuable tool for research in medicinal chemistry and drug development.
Presence of fluorine atoms
The presence of fluorine atoms in the compound may contribute to its stability, reactivity, and potential applications in imaging or analytical chemistry.
Check Digit Verification of cas no
The CAS Registry Mumber 143383-67-9 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,4,3,3,8 and 3 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 143383-67:
(8*1)+(7*4)+(6*3)+(5*3)+(4*8)+(3*3)+(2*6)+(1*7)=129
129 % 10 = 9
So 143383-67-9 is a valid CAS Registry Number.
143383-67-9Relevant articles and documents
Individual stereoisomers of pyrrolidine methanamines substituted on the ring nitrogen by a 1-phenylethyl group
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, (2008/06/13)
Individual stereoisomers of 7-[3-(1-aminoalkyl)-1-pyrrolidinyl]-quinolones and naphthyridones are described, their therapeutic advantages as antibacterial agents, as well as a novel method for the preparation and isolation of such stereoisomers.
