(S)-(4,4-Difluoropyrrolidin-2-yl)methanol hydrochloride
97%
- Product Code: 71078
CAS:
623583-10-8
| Molecular Weight: | 173.59 g./mol | Molecular Formula: | C₅H₁₀ClF₂NO |
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| EC Number: | MDL Number: | MFCD22570251 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | 2-8°C, sealed, dry |
Product Description:
(S)-(4,4-Difluoropyrrolidin-2-yl)methanol hydrochloride is primarily utilized in pharmaceutical research and development as a chiral building block. Its structure, featuring a difluorinated pyrrolidine ring, makes it valuable for synthesizing bioactive molecules, particularly in the design of drugs targeting the central nervous system (CNS). The compound’s chiral nature allows for the creation of enantiomerically pure substances, which is critical for optimizing drug efficacy and reducing side effects. It is often employed in the synthesis of potential therapeutic agents for neurological disorders, such as Parkinson’s disease or schizophrenia, due to its ability to interact with specific receptors or enzymes in the brain. Additionally, its fluorine atoms enhance metabolic stability and bioavailability, making it a preferred intermediate in medicinal chemistry.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿3,582.00 |
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(S)-(4,4-Difluoropyrrolidin-2-yl)methanol hydrochloride
(S)-(4,4-Difluoropyrrolidin-2-yl)methanol hydrochloride is primarily utilized in pharmaceutical research and development as a chiral building block. Its structure, featuring a difluorinated pyrrolidine ring, makes it valuable for synthesizing bioactive molecules, particularly in the design of drugs targeting the central nervous system (CNS). The compound’s chiral nature allows for the creation of enantiomerically pure substances, which is critical for optimizing drug efficacy and reducing side effects. It is often employed in the synthesis of potential therapeutic agents for neurological disorders, such as Parkinson’s disease or schizophrenia, due to its ability to interact with specific receptors or enzymes in the brain. Additionally, its fluorine atoms enhance metabolic stability and bioavailability, making it a preferred intermediate in medicinal chemistry.
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