(2R,4R)-4-Methylpiperidine-2-carboxylic acid

98%

Reagent Code: #230061
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CAS Number 74892-81-2

science Other reagents with same CAS 74892-81-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 143.18 g/mol
Formula C₇H₁₃NO₂
thermostat Physical Properties
Boiling Point 267°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its rigid piperidine scaffold with defined stereochemistry makes it valuable for drug design where spatial orientation affects biological activity. Commonly employed in medicinal chemistry for optimizing potency and selectivity in central nervous system agents and metabolic disease treatments. Also utilized in the preparation of enzyme inhibitors due to its ability to mimic amino acid structures in peptide-like compounds.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,400.00
inventory 1g
10-20 days ฿3,560.00

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(2R,4R)-4-Methylpiperidine-2-carboxylic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its rigid piperidine scaffold with defined stereochemistry makes it valuable for drug design where spatial orientation affects biological activity. Commonly employed in medicinal chemistry for optimizing potency and selectivity in central nervous system agents and metabolic disease treatments. Also utilized in the preparation of enzyme inhibitors due t

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its rigid piperidine scaffold with defined stereochemistry makes it valuable for drug design where spatial orientation affects biological activity. Commonly employed in medicinal chemistry for optimizing potency and selectivity in central nervous system agents and metabolic disease treatments. Also utilized in the preparation of enzyme inhibitors due to its ability to mimic amino acid structures in peptide-like compounds.

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