144551-23-5

Basic information

• Product Name: 2-[3(S)-[3-[2-(7 -Chloroquinoline-2-yl) Ethenyl] Pheny1]-3-Hydroxypropyl] phenyl methyl ketone
• Synonyms: 2-[3(S)-[3-[2-(7 -Chloroquinoline-2-yl) Ethenyl] Pheny1]-3-Hydroxypropyl] phenyl methyl ketone;(S,E)-1-(2-(3-(3-(2-(7-chloroquinolin-2-yl)vinyl)phenyl)-3-hydroxypropyl)phenyl)ethanone
• CAS NO: 144551-23-5
• Molecular Formula: C28H24 Cl N O2
• Molecular Weight: 441.95
• Mol File: 144551-23-5.mol
• Article Data: 0

Chemical Properties

• Appearance: /
• CAS DataBase Reference: 2-[3(S)-[3-[2-(7 -Chloroquinoline-2-yl) Ethenyl] Pheny1]-3-Hydroxypropyl] phenyl methyl ketone(CAS DataBase Reference)
• NIST Chemistry Reference: 2-[3(S)-[3-[2-(7 -Chloroquinoline-2-yl) Ethenyl] Pheny1]-3-Hydroxypropyl] phenyl methyl ketone(144551-23-5)
• EPA Substance Registry System: 2-[3(S)-[3-[2-(7 -Chloroquinoline-2-yl) Ethenyl] Pheny1]-3-Hydroxypropyl] phenyl methyl ketone(144551-23-5)

Safety Data

• Hazardous Substances Data: 144551-23-5(Hazardous Substances Data)

Usage

Properties

1. Chemical Class: Ketone
2. Functional Groups:
Quinoline ring
Phenyl group
3-hydroxypropyl side chain
3. Stereochemistry: Contains a chiral center denoted by (S), indicating the stereospecificity.
4. Medicinal Properties: Potential medicinal properties suitable for drug development.
5. Usage: Primarily used in the pharmaceutical industry.
6. Applications: Promising for the treatment of infectious diseases like malaria.
7. Structural Features: Unique chemical structure with a combination of quinoline ring, phenyl group, and a 3-hydroxypropyl side chain.
8. Research Interest: Subject of ongoing research in medicinal chemistry for exploring its therapeutic potential.

Specific Content

1. 2-[3(S)-[3-[2-(7-Chloroquinoline-2-yl)ethenyl]phenyl]-3-hydroxypropyl]phenyl methyl ketone
2-[3(S)-[3-[2-(7-Chloroquinoline-2-yl)ethenyl]phenyl]-3-hydroxypropyl]phenyl methyl ketone is the full chemical name.
2. Chemical Structure:
Contains a ketone functional group (C=O).
Quinoline ring structure.
Phenyl group attached to the 3-hydroxypropyl side chain.
Chloroquinoline-2-yl and ethenyl substituents.
3. Stereochemistry:
The (S) designation indicates the stereochemistry at a specific chiral center.
4. Medicinal Significance:
Potential for treating infectious diseases, especially malaria.
5. Pharmaceutical Industry Use:
Employed in drug development and medicinal chemistry research.
6. Therapeutic Potential:
Structure suggests possible activity against specific biological targets relevant to disease treatment.
7. Research Focus:
Subject of interest for further exploration in medicinal chemistry and pharmacology.
8. Structural Complexity:
Complex molecular structure with diverse functional groups, indicating potential versatility in interactions with biological targets.

This compound stands out for its unique structural features and potential applications in medicine, particularly in the development of drugs for combating infectious diseases like malaria. Further research and exploration are warranted to fully understand and harness its medicinal properties.