1-(5-Bromo-6-(trifluoromethyl)pyridin-3-yl)ethanone
95%
- Product Code: 39500
CAS:
1346252-30-9
Molecular Weight: | 268.0306 g./mol | Molecular Formula: | C₈H₅BrF₃NO |
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EC Number: | MDL Number: | MFCD26516942 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | room temperature |
Product Description:
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure, featuring a bromine atom and a trifluoromethyl group, makes it particularly valuable for constructing complex molecules with specific biological activities. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create compounds with potential therapeutic properties. Additionally, its presence in the synthesis of herbicides and pesticides highlights its importance in agricultural chemistry, where it contributes to the development of more effective crop protection agents. The compound’s unique reactivity also makes it a candidate for research in material science, particularly in the design of advanced organic materials.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.050 | 10-20 days | ฿8,451.00 |
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1-(5-Bromo-6-(trifluoromethyl)pyridin-3-yl)ethanone
This chemical is primarily utilized in the field of organic synthesis, where it serves as a key intermediate in the production of various pharmaceuticals and agrochemicals. Its structure, featuring a bromine atom and a trifluoromethyl group, makes it particularly valuable for constructing complex molecules with specific biological activities. It is often employed in cross-coupling reactions, such as Suzuki or Buchwald-Hartwig couplings, to create compounds with potential therapeutic properties. Additionally, its presence in the synthesis of herbicides and pesticides highlights its importance in agricultural chemistry, where it contributes to the development of more effective crop protection agents. The compound’s unique reactivity also makes it a candidate for research in material science, particularly in the design of advanced organic materials.
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