1-tert-butyl 2-Methyl (2R)-azetidine-1,2-dicarboxylate

97%

Reagent Code: #210378
fingerprint
CAS Number 1260593-39-2

science Other reagents with same CAS 1260593-39-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 215.25 g/mol
Formula C₁₀H₁₇NO₄
badge Registry Numbers
MDL Number MFCD11042210
inventory_2 Storage & Handling
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 enzyme inhibitors and bioactive molecules. Its protected azetidine core allows for selective functionalization, making it valuable in medicinal chemistry for constructing constrained ring systems that enhance metabolic stability and binding affinity. Commonly employed in asymmetric synthesis due to the stereochemical control it offers at the 2-position. Also utilized in the preparation of peptidomimetics and as an intermediate in the production of beta-lactamase inhibitors.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿1,330.00
inventory 1g
10-20 days ฿2,800.00
inventory 5g
10-20 days ฿10,000.00
inventory 10g
10-20 days ฿19,940.00
inventory 25g
10-20 days ฿43,340.00
1-tert-butyl 2-Methyl (2R)-azetidine-1,2-dicarboxylate
No image available

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of enzyme inhibitors and bioactive molecules. Its protected azetidine core allows for selective functionalization, making it valuable in medicinal chemistry for constructing constrained ring systems that enhance metabolic stability and binding affinity. Commonly employed in asymmetric synthesis due to the stereochemical control it offers at the 2-position. Also utilized in the preparation of peptidomimeti

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of enzyme inhibitors and bioactive molecules. Its protected azetidine core allows for selective functionalization, making it valuable in medicinal chemistry for constructing constrained ring systems that enhance metabolic stability and binding affinity. Commonly employed in asymmetric synthesis due to the stereochemical control it offers at the 2-position. Also utilized in the preparation of peptidomimetics and as an intermediate in the production of beta-lactamase inhibitors.

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...