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Catalog Number:
19276
CAS Number:
881841-42-5
8-Chloro-6-(trifluorométhyl)imidazo[1,2-a]pyridine-2-carbaldéhyde
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Product Information

8-Chloro-6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carbaldehyde is a versatile compound with significant applications in pharmaceutical research and development. This compound is recognized for its unique imidazo-pyridine structure, which contributes to its potential as a building block in the synthesis of various bioactive molecules. Its trifluoromethyl group enhances lipophilicity, making it an attractive candidate for drug design, particularly in the development of novel therapeutics targeting various diseases.

Researchers have utilized this compound in the synthesis of kinase inhibitors and other medicinal agents, showcasing its relevance in the pharmaceutical industry. Additionally, its ability to participate in diverse chemical reactions opens avenues for the creation of complex organic molecules, making it a valuable tool for chemists. With its distinctive properties and practical applications, 8-Chloro-6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carbaldehyde stands out as a key compound for those engaged in cutting-edge research and development.

CAS Number
881841-42-5
Molecular Formula
C9H4ClF3N2O
Molecular Weight
248.59
MDL Number
MFCD06739264
PubChem ID
28326410
Conditions
Conserver à 0-8°C
General Information
CAS Number
881841-42-5
Molecular Formula
C9H4ClF3N2O
Molecular Weight
248.59
MDL Number
MFCD06739264
PubChem ID
28326410
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

8-Chloro-6-(trifluoromethyl)imidazo[1,2-a]pyridine-2-carbaldehyde is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an important intermediate in the synthesis of various pharmaceuticals, particularly in developing anti-cancer agents due to its unique structural properties.
  • Agricultural Chemistry: It is used in the formulation of agrochemicals, enhancing the effectiveness of pesticides and herbicides, which helps in improving crop yield and pest management.
  • Material Science: The compound is explored for its potential in creating advanced materials with specific electronic and optical properties, beneficial for the development of new electronic devices.
  • Biochemical Research: It acts as a valuable tool in biochemical assays, allowing researchers to study enzyme interactions and cellular processes, which can lead to breakthroughs in understanding diseases.
  • Fluorinated Compound Synthesis: Its trifluoromethyl group makes it a key building block in the synthesis of other fluorinated compounds, which are often more stable and have unique reactivity compared to their non-fluorinated counterparts.

Citations