1-(tert-butyl) 3-methyl 3-fluoropyrrolidine-1,3-dicarboxylate
96%
- Product Code: 64500
CAS:
942189-96-0
| Molecular Weight: | 247.26 g./mol | Molecular Formula: | C₁₁H₁₈FNO₄ |
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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 versatile intermediate in the development of pharmaceuticals and bioactive molecules. Its structure, featuring both fluorinated and ester functional groups, makes it valuable for constructing complex molecules with specific steric and electronic properties. It is often employed in the synthesis of fluorinated pyrrolidine derivatives, which are key motifs in drug discovery due to their ability to enhance metabolic stability and binding affinity. Additionally, its tert-butyl ester group provides a protective moiety that can be selectively removed under mild conditions, facilitating stepwise synthetic strategies. This chemical is also explored in the preparation of agrochemicals and materials science applications, where its unique properties contribute to the development of novel compounds with tailored functionalities.
Product Specification:
| Test | Specification |
|---|---|
| APPEARANCE | Colorless liquid |
| PURITY | 95.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | Ft237,030.38 |
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| 5.000 | 10-20 days | Ft808,058.10 |
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1-(tert-butyl) 3-methyl 3-fluoropyrrolidine-1,3-dicarboxylate
This compound is primarily utilized in the field of organic synthesis, particularly as a versatile intermediate in the development of pharmaceuticals and bioactive molecules. Its structure, featuring both fluorinated and ester functional groups, makes it valuable for constructing complex molecules with specific steric and electronic properties. It is often employed in the synthesis of fluorinated pyrrolidine derivatives, which are key motifs in drug discovery due to their ability to enhance metabolic stability and binding affinity. Additionally, its tert-butyl ester group provides a protective moiety that can be selectively removed under mild conditions, facilitating stepwise synthetic strategies. This chemical is also explored in the preparation of agrochemicals and materials science applications, where its unique properties contribute to the development of novel compounds with tailored functionalities.
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