4-(4-Fluoro-benzoyl)-piperidine-1-carboxylic acid tert-butyl ester
95%
- Product Code: 83798
CAS:
160296-40-2
Molecular Weight: | 307.36 g./mol | Molecular Formula: | C₁₇H₂₂FNO₃ |
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EC Number: | MDL Number: | MFCD04114990 | |
Melting Point: | 80-83 °C | Boiling Point: | 410.4±35.0 °C(Predicted) |
Density: | 1.155±0.06 g/cm3(Predicted) | Storage Condition: | Room temperature, sealed, dry |
Product Description:
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of various biologically active molecules. Its structure, featuring a fluoro-benzoyl group and a piperidine ring, makes it valuable for the development of pharmaceutical agents, particularly those targeting neurological disorders and receptor modulation. It is often employed in the preparation of compounds that interact with the central nervous system, such as potential antipsychotics or analgesics. Additionally, its tert-butyl ester group provides stability during synthetic processes, making it a versatile building block in organic synthesis. Researchers also explore its use in creating novel drug candidates with improved efficacy and selectivity.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | ฿1,080.00 |
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0.250 | 10-20 days | ฿1,890.00 |
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1.000 | 10-20 days | ฿3,852.00 |
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4-(4-Fluoro-benzoyl)-piperidine-1-carboxylic acid tert-butyl ester
This compound is primarily utilized in the field of medicinal chemistry as an intermediate in the synthesis of various biologically active molecules. Its structure, featuring a fluoro-benzoyl group and a piperidine ring, makes it valuable for the development of pharmaceutical agents, particularly those targeting neurological disorders and receptor modulation. It is often employed in the preparation of compounds that interact with the central nervous system, such as potential antipsychotics or analgesics. Additionally, its tert-butyl ester group provides stability during synthetic processes, making it a versatile building block in organic synthesis. Researchers also explore its use in creating novel drug candidates with improved efficacy and selectivity.
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