(2R,4R)-1-(tert-butoxycarbonyl)-4-(difluoromethoxy)pyrrolidine-2-carboxylicacid

98%

Reagent Code: #232037
fingerprint
CAS Number 2381192-81-8

science Other reagents with same CAS 2381192-81-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 281.25 g/mol
Formula C₁₁H₁₇F₂NO₅
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors. Its chiral structure and functional groups make it valuable for constructing complex molecules with high stereoselectivity. Commonly employed in the preparation of antiviral and anticancer agents, where precise spatial arrangement of atoms is critical for biological activity. The Boc-protected amine and carboxylic acid allow for selective coupling reactions, enabling stepwise assembly of peptide-like structures. Its difluoromethoxy group enhances metabolic stability and membrane permeability in final drug candidates.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,490.00
inventory 250mg
10-20 days ฿14,980.00
inventory 1g
10-20 days ฿44,020.00
$product.analytical_desc - NULL

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(2R,4R)-1-(tert-butoxycarbonyl)-4-(difluoromethoxy)pyrrolidine-2-carboxylicacid
No image available

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors. Its chiral structure and functional groups make it valuable for constructing complex molecules with high stereoselectivity. Commonly employed in the preparation of antiviral and anticancer agents, where precise spatial arrangement of atoms is critical for biological activity. The Boc-protected amine and carboxylic acid allow for selective coupling reactions, enabling stepwise a

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors. Its chiral structure and functional groups make it valuable for constructing complex molecules with high stereoselectivity. Commonly employed in the preparation of antiviral and anticancer agents, where precise spatial arrangement of atoms is critical for biological activity. The Boc-protected amine and carboxylic acid allow for selective coupling reactions, enabling stepwise assembly of peptide-like structures. Its difluoromethoxy group enhances metabolic stability and membrane permeability in final drug candidates.

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...