tert-Butyl ((2S,4S,5S)-5-amino-4-hydroxy-1,6-diphenylhexan-2-yl)carbamate

98%

Reagent Code: #145934
fingerprint
CAS Number 144163-85-9

science Other reagents with same CAS 144163-85-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 384.51 g/mol
Formula C₂₃H₃₂N₂O₃
thermostat Physical Properties
Melting Point 71-74°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a protected intermediate in the synthesis of complex pharmaceuticals, particularly in the development of protease inhibitors. The tert-butyloxycarbonyl (Boc) group provides amine protection during peptide coupling reactions, allowing selective deprotection under mild acidic conditions. The stereochemistry supports the construction of chiral drug molecules, especially in HIV and hepatitis C antiviral agents. The hydroxyl and amine functionalities enable further derivatization, making it valuable in medicinal chemistry for building bioactive scaffolds.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿240.00
inventory 1g
10-20 days ฿870.00
inventory 5g
10-20 days ฿2,690.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
tert-Butyl ((2S,4S,5S)-5-amino-4-hydroxy-1,6-diphenylhexan-2-yl)carbamate
No image available

Used as a protected intermediate in the synthesis of complex pharmaceuticals, particularly in the development of protease inhibitors. The tert-butyloxycarbonyl (Boc) group provides amine protection during peptide coupling reactions, allowing selective deprotection under mild acidic conditions. The stereochemistry supports the construction of chiral drug molecules, especially in HIV and hepatitis C antiviral agents. The hydroxyl and amine functionalities enable further derivatization, making it valuable i

Used as a protected intermediate in the synthesis of complex pharmaceuticals, particularly in the development of protease inhibitors. The tert-butyloxycarbonyl (Boc) group provides amine protection during peptide coupling reactions, allowing selective deprotection under mild acidic conditions. The stereochemistry supports the construction of chiral drug molecules, especially in HIV and hepatitis C antiviral agents. The hydroxyl and amine functionalities enable further derivatization, making it valuable in medicinal chemistry for building bioactive scaffolds.

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...