tert-butyl (2S,4R)-4-hydroxy-2-methylpiperidine-1-carboxylate

≥98%

Reagent Code: #236160
fingerprint
CAS Number 790667-91-3

science Other reagents with same CAS 790667-91-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.29 g/mol
Formula C₁₁H₂₁NO₃
badge Registry Numbers
MDL Number MFCD21607787
thermostat Physical Properties
Boiling Point 281.9 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its protected hydroxyl and amine functionalities allow selective reactions in multi-step organic syntheses. The stereochemistry at the 2 and 4 positions enables precise control over the three-dimensional structure of the final drug molecule, enhancing biological activity and selectivity. Commonly employed in the preparation of HIV and HCV therapeutic candidates.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,550.00
inventory 250mg
10-20 days ฿10,450.00
inventory 1g
10-20 days ฿22,370.00
$product.analytical_desc - NULL

Cart

No products

Subtotal: 0.00
Total 0.00 THB
tert-butyl (2S,4R)-4-hydroxy-2-methylpiperidine-1-carboxylate
No image available

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its protected hydroxyl and amine functionalities allow selective reactions in multi-step organic syntheses. The stereochemistry at the 2 and 4 positions enables precise control over the three-dimensional structure of the final drug molecule, enhancing biological activity and selectivity. Commonly employed in the preparation of HIV and HCV therapeutic candidat

Used as a key chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and antiviral agents. Its protected hydroxyl and amine functionalities allow selective reactions in multi-step organic syntheses. The stereochemistry at the 2 and 4 positions enables precise control over the three-dimensional structure of the final drug molecule, enhancing biological activity and selectivity. Commonly employed in the preparation of HIV and HCV therapeutic candidates.

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...