(S)-4-(Benzyloxy)-2-(((benzyloxy)carbonyl)amino)butanoic acid

97%

Reagent Code: #232422
fingerprint
CAS Number 1356084-95-1

science Other reagents with same CAS 1356084-95-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 343.37 g/mol
Formula C₁₉H₂₁NO₅
badge Registry Numbers
MDL Number MFCD27998742
thermostat Physical Properties
Boiling Point 559.1±50.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.230±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its protected amino group and free carboxyl function, along with the protected side-chain hydroxy group, make it suitable for peptide coupling reactions, allowing selective formation of amide bonds in complex molecule assembly while preventing unwanted side reactions. Commonly employed in asymmetric synthesis due to its stereochemical purity, it helps introduce specific chirality in drug candidates. Also utilized in the preparation of enzyme inhibitors where precise spatial arrangement of functional groups is critical for biological activity.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿11,330.00
inventory 1g
10-20 days ฿51,870.00
(S)-4-(Benzyloxy)-2-(((benzyloxy)carbonyl)amino)butanoic acid
No image available

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its protected amino group and free carboxyl function, along with the protected side-chain hydroxy group, make it suitable for peptide coupling reactions, allowing selective formation of amide bonds in complex molecule assembly while preventing unwanted side reactions. Commonly employed in asymmetric synthesis due to its stereochemical purity, it helps

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its protected amino group and free carboxyl function, along with the protected side-chain hydroxy group, make it suitable for peptide coupling reactions, allowing selective formation of amide bonds in complex molecule assembly while preventing unwanted side reactions. Commonly employed in asymmetric synthesis due to its stereochemical purity, it helps introduce specific chirality in drug candidates. Also utilized in the preparation of enzyme inhibitors where precise spatial arrangement of functional groups 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...