(R)-2-Methylpiperidine-2-Carboxylic Acid

97%

Reagent Code: #231632
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CAS Number 105141-61-5

science Other reagents with same CAS 105141-61-5

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Weight 143.18 g/mol
Formula C₇H₁₃NO₂
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates requiring stereochemical control. Its rigid piperidine scaffold makes it valuable in medicinal chemistry for modulating the conformation of target compounds, enhancing selectivity and metabolic stability. Commonly employed in the preparation of enzyme inhibitors and receptor agonists/antagonists, especially in central nervous system and metabolic disorder research. Also utilized in asymmetric synthesis and catalysis due to its chiral amine functionality.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿16,800.00
(R)-2-Methylpiperidine-2-Carboxylic Acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates requiring stereochemical control. Its rigid piperidine scaffold makes it valuable in medicinal chemistry for modulating the conformation of target compounds, enhancing selectivity and metabolic stability. Commonly employed in the preparation of enzyme inhibitors and receptor agonists/antagonists, especially in central nervous system and metabolic disorder research.
Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates requiring stereochemical control. Its rigid piperidine scaffold makes it valuable in medicinal chemistry for modulating the conformation of target compounds, enhancing selectivity and metabolic stability. Commonly employed in the preparation of enzyme inhibitors and receptor agonists/antagonists, especially in central nervous system and metabolic disorder research. Also utilized in asymmetric synthesis and catalysis due to its chiral amine functionality.
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