(R)-tert-Butyl 3-(tosyloxy)pyrrolidine-1-carboxylate

95%

Reagent Code: #230184
fingerprint
CAS Number 139986-03-1

science Other reagents with same CAS 139986-03-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 341.42 g/mol
Formula C₁₆H₂₃NO₅S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its Boc-protected amine and activated tosylate group allow selective functionalization, making it valuable in multi-step organic syntheses. Commonly employed in the development of protease inhibitors and central nervous system agents. The compound’s stability and defined stereochemistry support its use in asymmetric synthesis and medicinal chemistry research.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,600.00
inventory 5g
10-20 days ฿7,970.00
inventory 25g
10-20 days ฿39,850.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(R)-tert-Butyl 3-(tosyloxy)pyrrolidine-1-carboxylate
No image available

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its Boc-protected amine and activated tosylate group allow selective functionalization, making it valuable in multi-step organic syntheses. Commonly employed in the development of protease inhibitors and central nervous system agents. The compound’s stability and defined stereochemistry support its use in asymmetric synthesis and

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the production of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its Boc-protected amine and activated tosylate group allow selective functionalization, making it valuable in multi-step organic syntheses. Commonly employed in the development of protease inhibitors and central nervous system agents. The compound’s stability and defined stereochemistry support its use in asymmetric synthesis and medicinal chemistry research.

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...