6,6-Difluorospiro[2.5]octane-1-carboxylic acid
95%
- Product Code: 66085
CAS:
1447943-53-4
| Molecular Weight: | 190.19 g./mol | Molecular Formula: | C₉H₁₂F₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD27995747 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8℃ |
Product Description:
6,6-Difluorospiro[2.5]octane-1-carboxylic acid is primarily used in the field of medicinal chemistry and drug development. Its unique spirocyclic structure and fluorine substitution make it a valuable building block for designing and synthesizing novel pharmaceutical compounds. The fluorine atoms enhance the molecule's metabolic stability and bioavailability, which is crucial for improving drug efficacy. This compound is often employed in the creation of small molecule inhibitors, particularly for targeting enzymes and receptors involved in various diseases. Additionally, its spirocyclic framework contributes to the exploration of three-dimensional chemical space, aiding in the discovery of compounds with improved selectivity and reduced off-target effects. Researchers also utilize it in the development of agrochemicals, where its structural properties can lead to the creation of more effective and environmentally friendly pesticides.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.250 | 10-20 days | ฿84,380.00 |
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| 1.000 | 10-20 days | ฿221,120.00 |
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6,6-Difluorospiro[2.5]octane-1-carboxylic acid
6,6-Difluorospiro[2.5]octane-1-carboxylic acid is primarily used in the field of medicinal chemistry and drug development. Its unique spirocyclic structure and fluorine substitution make it a valuable building block for designing and synthesizing novel pharmaceutical compounds. The fluorine atoms enhance the molecule's metabolic stability and bioavailability, which is crucial for improving drug efficacy. This compound is often employed in the creation of small molecule inhibitors, particularly for targeting enzymes and receptors involved in various diseases. Additionally, its spirocyclic framework contributes to the exploration of three-dimensional chemical space, aiding in the discovery of compounds with improved selectivity and reduced off-target effects. Researchers also utilize it in the development of agrochemicals, where its structural properties can lead to the creation of more effective and environmentally friendly pesticides.
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