(2S,4S)-1-((Benzyloxy)carbonyl)-4-hydroxypiperidine-2-carboxylic acid

95%

Reagent Code: #232618
fingerprint
CAS Number 441764-42-7

science Other reagents with same CAS 441764-42-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.3 g/mol
Formula C₁₄H₁₇NO₅
badge Registry Numbers
MDL Number MFCD27997475
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key chiral building block in the synthesis of pharmaceuticals, including protease inhibitors, CNS-active agents, and other bioactive molecules. The Cbz (benzyloxycarbonyl) group serves as a nitrogen protecting group, enabling selective modifications at the hydroxyl and carboxylic acid functional groups. This piperidine derivative is valuable in medicinal chemistry for constructing complex cyclic structures, peptide mimetics, and drug design where stereochemistry is critical for biological activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿9,580.00
inventory 100mg
10-20 days ฿16,290.00
inventory 250mg
10-20 days ฿27,680.00
(2S,4S)-1-((Benzyloxy)carbonyl)-4-hydroxypiperidine-2-carboxylic acid
No image available

Used as a key chiral building block in the synthesis of pharmaceuticals, including protease inhibitors, CNS-active agents, and other bioactive molecules. The Cbz (benzyloxycarbonyl) group serves as a nitrogen protecting group, enabling selective modifications at the hydroxyl and carboxylic acid functional groups. This piperidine derivative is valuable in medicinal chemistry for constructing complex cyclic structures, peptide mimetics, and drug design where stereochemistry is critical for biological activ

Used as a key chiral building block in the synthesis of pharmaceuticals, including protease inhibitors, CNS-active agents, and other bioactive molecules. The Cbz (benzyloxycarbonyl) group serves as a nitrogen protecting group, enabling selective modifications at the hydroxyl and carboxylic acid functional groups. This piperidine derivative is valuable in medicinal chemistry for constructing complex cyclic structures, peptide mimetics, and drug design where stereochemistry is critical for biological activity.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...