(R)-2-(Pyrrolidin-2-yl)propan-2-ol hydrochloride
95%
- Product Code: 37507
CAS:
816425-22-6
| Molecular Weight: | 165.66 g./mol | Molecular Formula: | C₇H₁₆ClNO |
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| EC Number: | MDL Number: | MFCD27952815 | |
| Melting Point: | Boiling Point: | ||
| Density: | Storage Condition: | room temperature, stored under inert gas |
Product Description:
(R)-2-(Pyrrolidin-2-yl)propan-2-ol hydrochloride is primarily used in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. It is particularly valuable in the development of chiral molecules, where its stereochemistry plays a critical role in enhancing the efficacy and selectivity of drugs. This compound is often employed in the production of active pharmaceutical ingredients (APIs) for treatments targeting central nervous system disorders, such as cognitive enhancers or antipsychotic medications. Additionally, its structural features make it a useful building block in the creation of ligands for receptor-binding studies, aiding in the discovery of new therapeutic agents. Its application extends to research in asymmetric synthesis, where it serves as a chiral auxiliary to control the stereochemistry of complex organic reactions.
Sizes / Availability / Pricing:
| Size (g) | Availability | Price | Quantity |
|---|---|---|---|
| 0.100 | 10-20 days | ฿1,368.00 |
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| 0.250 | 10-20 days | ฿2,745.00 |
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(R)-2-(Pyrrolidin-2-yl)propan-2-ol hydrochloride
(R)-2-(Pyrrolidin-2-yl)propan-2-ol hydrochloride is primarily used in the field of medicinal chemistry as a key intermediate in the synthesis of various pharmaceutical compounds. It is particularly valuable in the development of chiral molecules, where its stereochemistry plays a critical role in enhancing the efficacy and selectivity of drugs. This compound is often employed in the production of active pharmaceutical ingredients (APIs) for treatments targeting central nervous system disorders, such as cognitive enhancers or antipsychotic medications. Additionally, its structural features make it a useful building block in the creation of ligands for receptor-binding studies, aiding in the discovery of new therapeutic agents. Its application extends to research in asymmetric synthesis, where it serves as a chiral auxiliary to control the stereochemistry of complex organic reactions.
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