(R)-tert-Butyl (piperidin-3-ylmethyl)carbamate
97%
- Product Code: 113606
CAS:
879275-33-9
| Molecular Weight: | 214.31 g./mol | Molecular Formula: | C₁₁H₂₂N₂O₂ |
|---|---|---|---|
| EC Number: | MDL Number: | MFCD03093384 | |
| Melting Point: | Boiling Point: | 321.8±15.0°C at 760 mmHg | |
| Density: | Storage Condition: | 2-8°C, dry and sealed away from light |
Product Description:
This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active compounds. Its structure, featuring a piperidine ring and a carbamate group, makes it valuable for the development of drugs targeting the central nervous system. It is often employed in the creation of inhibitors for enzymes or receptors involved in neurological disorders, such as Alzheimer's disease or schizophrenia. Additionally, its chiral nature allows for the production of enantiomerically pure compounds, enhancing the specificity and efficacy of the resulting pharmaceuticals. Researchers also use it in the design of prodrugs, where its tert-butyl group can be cleaved under specific conditions to release the active drug molecule.
Product Specification:
| Test | Specification |
|---|---|
| Appearance | White To Yellow Solid |
| Purity (%) | 96.5-100 |
| Infrared Spectrum | Conforms To Structure |
| NMR | Conforms To Structure |
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 1.000 | 10-20 days | ฿2,260.00 |
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| 5.000 | 10-20 days | ฿8,660.00 |
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| 10.000 | 10-20 days | ฿15,880.00 |
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(R)-tert-Butyl (piperidin-3-ylmethyl)carbamate
This chemical is primarily utilized in the pharmaceutical industry as a key intermediate in the synthesis of various biologically active compounds. Its structure, featuring a piperidine ring and a carbamate group, makes it valuable for the development of drugs targeting the central nervous system. It is often employed in the creation of inhibitors for enzymes or receptors involved in neurological disorders, such as Alzheimer's disease or schizophrenia. Additionally, its chiral nature allows for the production of enantiomerically pure compounds, enhancing the specificity and efficacy of the resulting pharmaceuticals. Researchers also use it in the design of prodrugs, where its tert-butyl group can be cleaved under specific conditions to release the active drug molecule.
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