(3R,4R)-tert-Butyl4-amino-3-hydroxypiperidine-1-carboxylate

97%

Reagent Code: #231809
fingerprint
CAS Number 1007596-95-3

science Other reagents with same CAS 1007596-95-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 216.28 g/mol
Formula C₁₀H₂₀N₂O₃
badge Registry Numbers
MDL Number MFCD18072074
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and antiviral drugs. Its stereochemistry allows for high selectivity in biological targeting, making it valuable in constructing complex molecules with improved efficacy and reduced side effects. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where precise three-dimensional structure is critical for activity. Also utilized in medicinal chemistry research for optimizing drug candidates due to its stability and functional group compatibility in multi-step reactions.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,920.00
inventory 250mg
10-20 days ฿4,280.00
inventory 1g
10-20 days ฿14,080.00
inventory 5g
10-20 days ฿42,880.00
inventory 10g
10-20 days ฿80,000.00
(3R,4R)-tert-Butyl4-amino-3-hydroxypiperidine-1-carboxylate
No image available

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and antiviral drugs. Its stereochemistry allows for high selectivity in biological targeting, making it valuable in constructing complex molecules with improved efficacy and reduced side effects. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where precise three-dimensional structure is critical for activity. Also utilized in medicinal chemi

Used as a key chiral intermediate in the synthesis of pharmaceutical agents, particularly in the development of protease inhibitors and antiviral drugs. Its stereochemistry allows for high selectivity in biological targeting, making it valuable in constructing complex molecules with improved efficacy and reduced side effects. Commonly employed in the preparation of active pharmaceutical ingredients (APIs) where precise three-dimensional structure is critical for activity. Also utilized in medicinal chemistry research for optimizing drug candidates due to its stability and functional group compatibility in multi-step reactions.

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...