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Catalog Number:
44909
CAS Number:
18436-71-0
4-Chloro-6-methylquinoline
Purity:
≥ 98% (GC)
Documents
$215.62 /1G
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Product Information

4-Chloro-6-methylquinoline is a versatile compound recognized for its significant role in various chemical syntheses and applications. This heterocyclic aromatic compound, characterized by its chlorine and methyl substituents, is widely utilized in the pharmaceutical industry for the development of novel therapeutic agents. Its unique structure allows for the modification of biological activity, making it a valuable building block in the synthesis of quinoline derivatives, which are known for their antimicrobial, antimalarial, and anti-inflammatory properties. Researchers often leverage 4-Chloro-6-methylquinoline in the design of targeted drug delivery systems and in the exploration of new medicinal chemistry pathways.

In addition to its pharmaceutical applications, 4-Chloro-6-methylquinoline is also employed in agrochemical formulations, contributing to the development of effective pesticides and herbicides. Its stability and reactivity make it an ideal candidate for various chemical reactions, including nucleophilic substitutions and cyclization processes. With its broad applicability and potential for innovation, 4-Chloro-6-methylquinoline stands out as a compound of interest for both researchers and industry professionals seeking to enhance their product offerings or explore new avenues in chemical research.

CAS Number
18436-71-0
Purity
≥ 98% (GC)
Molecular Formula
C10H8ClN
Molecular Weight
177.63
MDL Number
MFCD02684204
PubChem ID
824624
Melting Point
51 - 55 °C
Appearance
Light orange to yellow to green powder to crystal
Boiling Point
140 °C/10 mmHg
Conditions
Store at RT
General Information
CAS Number
18436-71-0
Purity
≥ 98% (GC)
Molecular Formula
C10H8ClN
Molecular Weight
177.63
MDL Number
MFCD02684204
PubChem ID
824624
Melting Point
51 - 55 °C
Appearance
Light orange to yellow to green powder to crystal
Boiling Point
140 °C/10 mmHg
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Chloro-6-methylquinoline is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-inflammatory and antimicrobial agents.
  • Biological Research: It is used in studies investigating the mechanisms of action of quinoline derivatives, contributing to the understanding of their biological activities and potential therapeutic effects.
  • Agricultural Chemistry: The compound is explored for its potential as a pesticide or herbicide, helping to develop safer and more effective agricultural products.
  • Material Science: 4-Chloro-6-methylquinoline is investigated for its properties in creating specialized coatings and polymers, enhancing material performance in various applications.
  • Analytical Chemistry: It is employed as a reagent in analytical methods, aiding in the detection and quantification of other chemical substances in complex mixtures.

Citations