1-Boc-4-oxo-D-proline benzyl ester

95%

Reagent Code: #63845
fingerprint
CAS Number 224627-26-3

science Other reagents with same CAS 224627-26-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 319.35 g/mol
Formula C₁₇H₂₁NO₅
badge Registry Numbers
MDL Number MFCD18252787
thermostat Physical Properties
Boiling Point 439.9±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.219±0.06 g/cm3(Predicted)
Storage -20°C, sealed, dry

description Product Description

Used in the synthesis of complex organic molecules, particularly in the pharmaceutical industry for the production of peptide-based drugs. It serves as a key intermediate in the preparation of proline derivatives, which are essential in designing protease inhibitors and other bioactive compounds. Its Boc-protected group ensures selective reactions during multi-step synthesis, while the benzyl ester facilitates controlled deprotection. This compound is also valuable in research for developing new therapeutic agents targeting diseases like cancer and viral infections.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,574.00
inventory 1g
10-20 days ฿9,360.00
inventory 250mg
10-20 days ฿4,680.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1-Boc-4-oxo-D-proline benzyl ester
No image available

Used in the synthesis of complex organic molecules, particularly in the pharmaceutical industry for the production of peptide-based drugs. It serves as a key intermediate in the preparation of proline derivatives, which are essential in designing protease inhibitors and other bioactive compounds. Its Boc-protected group ensures selective reactions during multi-step synthesis, while the benzyl ester facilitates controlled deprotection. This compound is also valuable in research for developing new therapeu

Used in the synthesis of complex organic molecules, particularly in the pharmaceutical industry for the production of peptide-based drugs. It serves as a key intermediate in the preparation of proline derivatives, which are essential in designing protease inhibitors and other bioactive compounds. Its Boc-protected group ensures selective reactions during multi-step synthesis, while the benzyl ester facilitates controlled deprotection. This compound is also valuable in research for developing new therapeutic agents targeting diseases like cancer and viral infections.

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...