1-Boc-4-cyano-2,2-dimethyl-3-oxopyrrolidine

95%

Reagent Code: #149856
fingerprint
CAS Number 718632-42-9

science Other reagents with same CAS 718632-42-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 238.3 g/mol
Formula C₁₂H₁₈N₂O₃
badge Registry Numbers
MDL Number MFCD08275049
inventory_2 Storage & Handling
Storage 2-8°C, dry, closed

description Product Description

Used in pharmaceutical synthesis as a key intermediate for constructing complex heterocyclic compounds, particularly in the development of bioactive molecules and drug candidates. Its protected amine group (Boc) allows selective reactivity, while the cyano and ketone functionalities enable further transformations such as reductions, nucleophilic additions, and cyclization reactions. Commonly employed in the synthesis of protease inhibitors and other therapeutic agents where pyrrolidine scaffolds are structural motifs. The presence of geminal dimethyl groups enhances steric stability and influences conformational rigidity in the final active compound.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,670.00
inventory 250mg
10-20 days ฿13,020.00
inventory 1g
10-20 days ฿43,110.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
1-Boc-4-cyano-2,2-dimethyl-3-oxopyrrolidine
No image available

Used in pharmaceutical synthesis as a key intermediate for constructing complex heterocyclic compounds, particularly in the development of bioactive molecules and drug candidates. Its protected amine group (Boc) allows selective reactivity, while the cyano and ketone functionalities enable further transformations such as reductions, nucleophilic additions, and cyclization reactions. Commonly employed in the synthesis of protease inhibitors and other therapeutic agents where pyrrolidine scaffolds are stru

Used in pharmaceutical synthesis as a key intermediate for constructing complex heterocyclic compounds, particularly in the development of bioactive molecules and drug candidates. Its protected amine group (Boc) allows selective reactivity, while the cyano and ketone functionalities enable further transformations such as reductions, nucleophilic additions, and cyclization reactions. Commonly employed in the synthesis of protease inhibitors and other therapeutic agents where pyrrolidine scaffolds are structural motifs. The presence of geminal dimethyl groups enhances steric stability and influences conformational rigidity in the final active compound.

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...