(1S,2S)-2-(4-Fluoro-phenyl)-cyclopropanecarboxylic acid
97%
- Product Code: 36251
CAS:
515179-19-8
| Molecular Weight: | 180.18 g./mol | Molecular Formula: | C₁₀H₉FO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | ||
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature |
Product Description:
(1S,2S)-2-(4-Fluoro-phenyl)-cyclopropanecarboxylic acid is primarily utilized in the field of medicinal chemistry and pharmaceutical research. Its unique cyclopropane ring structure, combined with the presence of a fluorine atom, makes it a valuable intermediate in the synthesis of biologically active compounds. It is often employed in the development of drug candidates, particularly those targeting central nervous system disorders, due to its ability to modulate specific receptors or enzymes. Additionally, its structural features are explored in the design of inhibitors for various enzymes, contributing to the study of metabolic pathways and disease mechanisms. The compound's chiral nature also makes it useful in asymmetric synthesis, enabling the production of enantiomerically pure pharmaceuticals.
Product Specification:
| Test | Specification |
|---|---|
| PURITY | 96.5-100 |
| Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿6,300.00 |
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| 0.250 | 10-20 days | ฿12,600.00 |
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(1S,2S)-2-(4-Fluoro-phenyl)-cyclopropanecarboxylic acid
(1S,2S)-2-(4-Fluoro-phenyl)-cyclopropanecarboxylic acid is primarily utilized in the field of medicinal chemistry and pharmaceutical research. Its unique cyclopropane ring structure, combined with the presence of a fluorine atom, makes it a valuable intermediate in the synthesis of biologically active compounds. It is often employed in the development of drug candidates, particularly those targeting central nervous system disorders, due to its ability to modulate specific receptors or enzymes. Additionally, its structural features are explored in the design of inhibitors for various enzymes, contributing to the study of metabolic pathways and disease mechanisms. The compound's chiral nature also makes it useful in asymmetric synthesis, enabling the production of enantiomerically pure pharmaceuticals.
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