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Catalog Number:
18703
CAS Number:
124467-20-5
2-Chloro-6-iodo-quinoline
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Product Information

2-Chloro-6-iodo-quinoline is a versatile chemical compound recognized for its significant applications in pharmaceutical research and development. This compound features a unique halogenated structure that enhances its reactivity, making it a valuable intermediate in the synthesis of various bioactive molecules. Researchers utilize 2-Chloro-6-iodo-quinoline in the development of novel therapeutic agents, particularly in the fields of oncology and infectious diseases, where it has shown potential as a lead compound for drug discovery. Its ability to act as a building block in complex organic synthesis allows for the creation of diverse derivatives, expanding its utility in medicinal chemistry.

Moreover, 2-Chloro-6-iodo-quinoline stands out due to its favorable properties, such as good solubility in organic solvents and stability under various conditions, which are crucial for laboratory applications. Its unique combination of chlorine and iodine substituents contributes to its reactivity profile, making it an attractive candidate for further functionalization. This compound not only facilitates the exploration of new chemical entities but also supports the advancement of innovative solutions in drug development, thereby addressing critical health challenges.

CAS Number
124467-20-5
Molecular Formula
C9H5ClIN
Molecular Weight
289.5
MDL Number
MFCD04115269
PubChem ID
19898697
Conditions
Store at 0-8°C
General Information
CAS Number
124467-20-5
Molecular Formula
C9H5ClIN
Molecular Weight
289.5
MDL Number
MFCD04115269
PubChem ID
19898697
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Chloro-6-iodo-quinoline is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in developing anti-cancer agents and antimicrobial drugs.
  • Biological Research: It is used in studies investigating the mechanisms of action of quinoline derivatives, helping researchers understand their biological activity and potential therapeutic effects.
  • Material Science: The compound is explored for its properties in creating advanced materials, including organic semiconductors and dyes, which are essential in electronics and coatings.
  • Agricultural Chemistry: It finds applications in developing agrochemicals, particularly as a precursor for pesticides that target specific pests while minimizing environmental impact.
  • Analytical Chemistry: This chemical is employed in analytical methods for detecting and quantifying quinoline derivatives in various samples, aiding quality control in pharmaceutical manufacturing.

Citations