(S)-Dibenzyl 2-aminosuccinate

95%

Reagent Code: #232656
fingerprint
CAS Number 2791-79-9

science Other reagents with same CAS 2791-79-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 313.35 g/mol
Formula C₁₈H₁₉NO₄
badge Registry Numbers
MDL Number MFCD09749710
inventory_2 Storage & Handling
Storage -20°C, light-proof, inert gas

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 stereochemistry makes it valuable for asymmetric synthesis, where it helps control the formation of specific enantiomers in drug intermediates. Commonly employed in peptide mimetics and as a precursor in the preparation of nitrogen-containing heterocycles. The benzyl protecting groups allow for selective deprotection and further functionalization in multi-step synthetic routes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,560.00
inventory 1g
10-20 days ฿6,920.00
(S)-Dibenzyl 2-aminosuccinate
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 stereochemistry makes it valuable for asymmetric synthesis, where it helps control the formation of specific enantiomers in drug intermediates. Commonly employed in peptide mimetics and as a precursor in the preparation of nitrogen-containing heterocycles. The benzyl protecting groups allow for selective deprotection and further functionalization i

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of protease inhibitors and other bioactive molecules. Its stereochemistry makes it valuable for asymmetric synthesis, where it helps control the formation of specific enantiomers in drug intermediates. Commonly employed in peptide mimetics and as a precursor in the preparation of nitrogen-containing heterocycles. The benzyl protecting groups allow for selective deprotection and further functionalization in multi-step synthetic routes.

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...