(R)-Quinuclidin-3-amine
98%
- Product Code: 37773
CAS:
123536-15-2
Molecular Weight: | 126.1995 g./mol | Molecular Formula: | C₇H₁₄N₂ |
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EC Number: | MDL Number: | MFCD08669630 | |
Melting Point: | Boiling Point: | ||
Density: | Storage Condition: | 2-8°C |
Product Description:
(R)-Quinuclidin-3-amine is primarily used as a chiral building block in the synthesis of various pharmaceutical compounds. Its rigid bicyclic structure and chiral center make it valuable for designing molecules with specific stereochemical properties. It is often employed in the development of drugs targeting the central nervous system, such as antipsychotics and antidepressants, due to its ability to interact with neurotransmitter receptors. Additionally, it serves as a key intermediate in the production of ligands for G-protein-coupled receptors (GPCRs), which are critical in drug discovery for treating conditions like pain, inflammation, and cardiovascular diseases. Its versatility in organic synthesis also extends to creating catalysts and chiral auxiliaries for asymmetric synthesis, enhancing the efficiency and selectivity of chemical reactions.
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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0.100 | 10-20 days | $162.28 |
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(R)-Quinuclidin-3-amine
(R)-Quinuclidin-3-amine is primarily used as a chiral building block in the synthesis of various pharmaceutical compounds. Its rigid bicyclic structure and chiral center make it valuable for designing molecules with specific stereochemical properties. It is often employed in the development of drugs targeting the central nervous system, such as antipsychotics and antidepressants, due to its ability to interact with neurotransmitter receptors. Additionally, it serves as a key intermediate in the production of ligands for G-protein-coupled receptors (GPCRs), which are critical in drug discovery for treating conditions like pain, inflammation, and cardiovascular diseases. Its versatility in organic synthesis also extends to creating catalysts and chiral auxiliaries for asymmetric synthesis, enhancing the efficiency and selectivity of chemical reactions.
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