(2S,5S)-5-Hydroxypiperidine-2-carboxylic acid

95%

Reagent Code: #235631
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Alias Related CAS number: 154307-84-3
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CAS Number 63088-78-8

science Other reagents with same CAS 63088-78-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 145.16 g/mol
Formula C₆H₁₁NO₃
badge Registry Numbers
MDL Number MFCD19217172
thermostat Physical Properties
Boiling Point 354.8°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, dry and sealed from light

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of enzyme inhibitors and bioactive molecules. Its rigid piperidine scaffold with defined stereochemistry makes it valuable in medicinal chemistry for designing drugs targeting neurological disorders and metabolic diseases. Also employed in the preparation of peptidomimetics due to its structural similarity to proline, enhancing stability and specificity in peptide-based therapeutics.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,680.00
inventory 250mg
10-20 days ฿3,880.00
inventory 1g
10-20 days ฿11,880.00
(2S,5S)-5-Hydroxypiperidine-2-carboxylic acid
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Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of enzyme inhibitors and bioactive molecules. Its rigid piperidine scaffold with defined stereochemistry makes it valuable in medicinal chemistry for designing drugs targeting neurological disorders and metabolic diseases. Also employed in the preparation of peptidomimetics due to its structural similarity to proline, enhancing stability and specificity in peptide-based therapeutics.

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of enzyme inhibitors and bioactive molecules. Its rigid piperidine scaffold with defined stereochemistry makes it valuable in medicinal chemistry for designing drugs targeting neurological disorders and metabolic diseases. Also employed in the preparation of peptidomimetics due to its structural similarity to proline, enhancing stability and specificity in peptide-based therapeutics.

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