ethyl 2-(5-bromopyridin-2-yl)-2,2-difluoroacetate
90%
- Product Code: 74624
CAS:
294181-95-6
Molecular Weight: | 280.07 g./mol | Molecular Formula: | C₉H₈BrF₂NO₂ |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8℃ |
Product Description:
This compound is primarily utilized in the field of organic synthesis, particularly as a building block for the development of more complex molecules. Its structure, featuring a bromopyridine moiety and difluoroacetate group, makes it valuable in the creation of pharmaceuticals and agrochemicals. The bromine atom serves as a reactive site for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, enabling the synthesis of diverse heterocyclic compounds. Additionally, the difluoroacetate group can influence the metabolic stability and bioavailability of the resulting compounds, making it useful in drug discovery and optimization processes. Its applications also extend to materials science, where it can be used to design novel organic materials with specific electronic or optical properties.
Product Specification:
Test | Specification |
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APPEARANCE | Colourless to Yellow |
PURITY | 94.5-100 |
Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿3,170.00 |
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0.500 | 10-20 days | ฿8,820.00 |
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1.000 | 10-20 days | ฿11,760.00 |
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ethyl 2-(5-bromopyridin-2-yl)-2,2-difluoroacetate
This compound is primarily utilized in the field of organic synthesis, particularly as a building block for the development of more complex molecules. Its structure, featuring a bromopyridine moiety and difluoroacetate group, makes it valuable in the creation of pharmaceuticals and agrochemicals. The bromine atom serves as a reactive site for further functionalization through cross-coupling reactions, such as Suzuki or Buchwald-Hartwig reactions, enabling the synthesis of diverse heterocyclic compounds. Additionally, the difluoroacetate group can influence the metabolic stability and bioavailability of the resulting compounds, making it useful in drug discovery and optimization processes. Its applications also extend to materials science, where it can be used to design novel organic materials with specific electronic or optical properties.
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