2-[(4R)-4-tert-Butyl-4,5-dihydro-2-oxazolyl]-5-(trifluoromethyl)pyridine
≥98%,99%e.e.
- Product Code: 70611
CAS:
1428537-19-2
Molecular Weight: | 272.3 g./mol | Molecular Formula: | C₁₃H₁₅F₃N₂O |
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EC Number: | MDL Number: | ||
Melting Point: | Boiling Point: | 319.6±42.0 °C | |
Density: | 1.25±0.1 g/mL | Storage Condition: | room temperature, dry |
Product Description:
This compound is primarily utilized in the field of organic synthesis as a key intermediate or building block for the development of more complex molecules. Its structure, featuring a trifluoromethyl group and an oxazoline ring, makes it particularly valuable in the synthesis of pharmaceuticals and agrochemicals. The trifluoromethyl group enhances the biological activity and metabolic stability of the final compounds, while the oxazoline ring can act as a chiral auxiliary or ligand in asymmetric catalysis. Additionally, it is employed in research settings for the design and optimization of novel chemical entities with potential therapeutic or agricultural applications. Its unique properties contribute to the development of compounds with improved efficacy and selectivity.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.050 | 10-20 days | ฿1,251.00 |
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2-[(4R)-4-tert-Butyl-4,5-dihydro-2-oxazolyl]-5-(trifluoromethyl)pyridine
This compound is primarily utilized in the field of organic synthesis as a key intermediate or building block for the development of more complex molecules. Its structure, featuring a trifluoromethyl group and an oxazoline ring, makes it particularly valuable in the synthesis of pharmaceuticals and agrochemicals. The trifluoromethyl group enhances the biological activity and metabolic stability of the final compounds, while the oxazoline ring can act as a chiral auxiliary or ligand in asymmetric catalysis. Additionally, it is employed in research settings for the design and optimization of novel chemical entities with potential therapeutic or agricultural applications. Its unique properties contribute to the development of compounds with improved efficacy and selectivity.
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