1-(2,5-difluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanone

98%

  • Product Code: 39144
  CAS:    1157938-97-0
Molecular Weight: 669.54 g./mol Molecular Formula: C₃₀H₂₁F₆N₉O₃
EC Number: MDL Number:
Melting Point: Boiling Point:
Density: Storage Condition: 2-8°C
Product Description: This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structure, featuring a difluorophenyl group and a triazole moiety, makes it a valuable building block for developing antifungal and antimicrobial drugs. The triazole ring is particularly significant due to its ability to interact with biological targets, such as enzymes involved in fungal cell wall synthesis, making it effective in treating fungal infections. Additionally, the difluorophenyl group enhances the compound's stability and bioavailability, which is crucial for drug development. Researchers also explore its potential in designing compounds for other therapeutic areas, including anti-inflammatory and anticancer agents, due to its versatile chemical reactivity.
Product Specification:
Test Specification
APPEARANCE White to Yellow solid
PURITY 97.5-100
Infrared spectrum Conforms to Structure
NMR Conforms to Structure
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
1.000 10-20 days $280.26
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1-(2,5-difluorophenyl)-2-(1H-1,2,4-triazol-1-yl)ethanone
This compound is primarily utilized in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical agents. Its structure, featuring a difluorophenyl group and a triazole moiety, makes it a valuable building block for developing antifungal and antimicrobial drugs. The triazole ring is particularly significant due to its ability to interact with biological targets, such as enzymes involved in fungal cell wall synthesis, making it effective in treating fungal infections. Additionally, the difluorophenyl group enhances the compound's stability and bioavailability, which is crucial for drug development. Researchers also explore its potential in designing compounds for other therapeutic areas, including anti-inflammatory and anticancer agents, due to its versatile chemical reactivity.
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