(2R,3S)-3-((tert-Butoxycarbonyl)amino)-2-hydroxy-4-phenylbutanoic acid

98%

Reagent Code: #232380
fingerprint
CAS Number 105181-72-4

science Other reagents with same CAS 105181-72-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 295.33 g/mol
Formula C₁₅H₂₁NO₅
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of protease inhibitors such as those used in antiviral therapies. Its stereochemistry allows for selective binding in enzyme active sites, making it valuable in the development of drugs targeting HIV and hepatitis C. The Boc-protected amine and carboxylic acid functionality enable stepwise peptide coupling, facilitating its incorporation into complex peptide-based molecules. Commonly employed in research and industrial settings for solid-phase and solution-phase peptide synthesis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿77,190.00
(2R,3S)-3-((tert-Butoxycarbonyl)amino)-2-hydroxy-4-phenylbutanoic acid
No image available

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of protease inhibitors such as those used in antiviral therapies. Its stereochemistry allows for selective binding in enzyme active sites, making it valuable in the development of drugs targeting HIV and hepatitis C. The Boc-protected amine and carboxylic acid functionality enable stepwise peptide coupling, facilitating its incorporation into complex peptide-based molecules. Commonly employed in research and

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of protease inhibitors such as those used in antiviral therapies. Its stereochemistry allows for selective binding in enzyme active sites, making it valuable in the development of drugs targeting HIV and hepatitis C. The Boc-protected amine and carboxylic acid functionality enable stepwise peptide coupling, facilitating its incorporation into complex peptide-based molecules. Commonly employed in research and industrial settings for solid-phase and solution-phase peptide synthesis.

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...