(S)-Benzyl 2-(aminomethyl)pyrrolidine-1-carboxylate

98%

Reagent Code: #236748
fingerprint
CAS Number 141774-68-7

science Other reagents with same CAS 141774-68-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 234.3 g/mol
Formula C₁₃H₁₈N₂O₂
badge Registry Numbers
MDL Number MFCD03093059
inventory_2 Storage & Handling
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure supports the creation of complex amines found in bioactive molecules. Commonly employed in medicinal chemistry for drug discovery, especially in central nervous system (CNS) agents and enzyme inhibitors. The benzyl carbamate group acts as a protecting group for the amine, allowing selective reactions at other functional sites during multi-step syntheses. Its pyrrolidine core is valuable in crafting conformationally restricted analogs to enhance binding affinity and metabolic stability in drug candidates.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿680.00
inventory 250mg
10-20 days ฿1,120.00
inventory 10g
10-20 days ฿15,200.00
inventory 1g
10-20 days ฿2,340.00
(S)-Benzyl 2-(aminomethyl)pyrrolidine-1-carboxylate
No image available

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure supports the creation of complex amines found in bioactive molecules. Commonly employed in medicinal chemistry for drug discovery, especially in central nervous system (CNS) agents and enzyme inhibitors. The benzyl carbamate group acts as a protecting group for the amine, allowing selective reactions at other fun

Used as a chiral building block in the synthesis of pharmaceuticals, particularly in the development of active pharmaceutical ingredients (APIs) requiring high enantiomeric purity. Its structure supports the creation of complex amines found in bioactive molecules. Commonly employed in medicinal chemistry for drug discovery, especially in central nervous system (CNS) agents and enzyme inhibitors. The benzyl carbamate group acts as a protecting group for the amine, allowing selective reactions at other functional sites during multi-step syntheses. Its pyrrolidine core is valuable in crafting conformationally restricted analogs to enhance binding affinity and metabolic stability in 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...