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Catalog Number:
25876
CAS Number:
1701-24-2
2-Trifluoromethyl-4-chloroquinoline
Purity:
≥ 98% (Assay)
Synonym(s):
4-Chloro-2-(trifluoromethyl)quinoline
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Product Information

2-Trifluoromethyl-4-chloroquinoline is a versatile compound known for its unique trifluoromethyl and chloro substituents, which enhance its reactivity and biological activity. This compound is particularly valuable in the pharmaceutical industry, where it serves as a key intermediate in the synthesis of various bioactive molecules, including potential anti-cancer and anti-inflammatory agents. Its distinct structure allows for modifications that can lead to the development of novel therapeutic compounds, making it a crucial building block for medicinal chemistry research.

In addition to its pharmaceutical applications, 2-Trifluoromethyl-4-chloroquinoline is also utilized in agrochemical formulations, where it contributes to the development of effective pesticides and herbicides. The compound's stability and reactivity make it an ideal candidate for further research and development in both academic and industrial settings. Researchers and industry professionals can leverage its unique properties to innovate and enhance product efficacy, ultimately leading to improved outcomes in various applications.

Synonyms
4-Chloro-2-(trifluoromethyl)quinoline
CAS Number
1701-24-2
Purity
≥ 98% (Assay)
Molecular Formula
C10H5ClF3N
Molecular Weight
231.6
MDL Number
MFCD00153105
PubChem ID
2736709
Melting Point
35 - 43 ?C
Appearance
Pale yellow to white crystalline solid
Conditions
Store at 0 - 8 °C
General Information
Synonyms
4-Chloro-2-(trifluoromethyl)quinoline
CAS Number
1701-24-2
Purity
≥ 98% (Assay)
Molecular Formula
C10H5ClF3N
Molecular Weight
231.6
MDL Number
MFCD00153105
PubChem ID
2736709
Melting Point
35 - 43 ?C
Appearance
Pale yellow to white crystalline solid
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Trifluoromethyl-4-chloroquinoline 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 antimalarial and antibacterial agents. Its unique structure enhances biological activity, making it a valuable asset in drug discovery.
  • Agricultural Chemicals: It is used in formulating agrochemicals, including pesticides and herbicides. The trifluoromethyl group improves the efficacy and stability of these products, offering better protection against pests and diseases in crops.
  • Material Science: The compound is explored in creating advanced materials, particularly in coatings and polymers. Its chemical properties contribute to improved durability and resistance to environmental factors, making it suitable for various industrial applications.
  • Research Reagents: As a reagent, it is employed in organic synthesis and analytical chemistry. Its distinct characteristics allow researchers to develop new methodologies and improve existing ones, facilitating advancements in chemical research.
  • Fluorine Chemistry: The presence of fluorine in its structure makes it a subject of interest in fluorine chemistry studies. Researchers investigate its reactivity and potential applications in creating novel fluorinated compounds, which are increasingly important in various fields.

Citations