(S)-tert-Butyl (5-oxopyrrolidin-3-yl)carbamate

95%

Reagent Code: #234973
fingerprint
CAS Number 672883-23-7

science Other reagents with same CAS 672883-23-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 200.24 g/mol
Formula C₉H₁₆N₂O₃
thermostat Physical Properties
Boiling Point 394°C
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of neuroactive compounds and enzyme inhibitors. Its protected amine and ketone functional groups allow for selective reactions, making it valuable in asymmetric synthesis. Commonly employed in the preparation of pyrrolidine-based drugs targeting central nervous system disorders and metabolic diseases. The stereochemistry supports high enantioselectivity in final active ingredients.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,600.00
inventory 250mg
10-20 days ฿7,400.00
inventory 1g
10-20 days ฿19,200.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
(S)-tert-Butyl (5-oxopyrrolidin-3-yl)carbamate
No image available

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of neuroactive compounds and enzyme inhibitors. Its protected amine and ketone functional groups allow for selective reactions, making it valuable in asymmetric synthesis. Commonly employed in the preparation of pyrrolidine-based drugs targeting central nervous system disorders and metabolic diseases. The stereochemistry supports high enantioselectivity in final active ingredients.

Used as a chiral intermediate in the synthesis of pharmaceuticals, particularly in the development of neuroactive compounds and enzyme inhibitors. Its protected amine and ketone functional groups allow for selective reactions, making it valuable in asymmetric synthesis. Commonly employed in the preparation of pyrrolidine-based drugs targeting central nervous system disorders and metabolic diseases. The stereochemistry supports high enantioselectivity in final active ingredients.

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...