3-Fluorobicyclo[1.1.1]pentane-1-carboxylic acid
98%
- Product Code: 65944
CAS:
146038-53-1
| Molecular Weight: | 130.12 g./mol | Molecular Formula: | C₆H₇FO₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD19228680 | |
| Melting Point: | 117-118 °C | Boiling Point: | 217.0±40.0 °C(Predicted) |
| Density: | 1.42±0.1 g/cm3(Predicted) | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry and drug discovery. It serves as a valuable building block for the synthesis of biologically active molecules, particularly in the development of pharmaceuticals. The unique structure of the bicyclo[1.1.1]pentane ring system, combined with the fluorine substituent, enhances the metabolic stability and bioavailability of drug candidates. It is often incorporated into small molecules to improve their pharmacokinetic properties and target specificity. Additionally, its application extends to the design of peptide mimetics and enzyme inhibitors, where it helps mimic natural substrates while providing enhanced resistance to enzymatic degradation.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿2,925.00 |
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| 0.250 | 10-20 days | ฿5,778.00 |
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| 1.000 | 10-20 days | ฿15,300.00 |
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3-Fluorobicyclo[1.1.1]pentane-1-carboxylic acid
This compound is primarily utilized in the field of medicinal chemistry and drug discovery. It serves as a valuable building block for the synthesis of biologically active molecules, particularly in the development of pharmaceuticals. The unique structure of the bicyclo[1.1.1]pentane ring system, combined with the fluorine substituent, enhances the metabolic stability and bioavailability of drug candidates. It is often incorporated into small molecules to improve their pharmacokinetic properties and target specificity. Additionally, its application extends to the design of peptide mimetics and enzyme inhibitors, where it helps mimic natural substrates while providing enhanced resistance to enzymatic degradation.
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