Tert-Butyl 3,3-Dimethyl-2-Oxopyrrolidine-1-Carboxylate

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Reagent Code: #83456
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CAS Number 153039-16-8

science Other reagents with same CAS 153039-16-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 213.27 g/mol
Formula C₁₁H₁₉NO₃
badge Registry Numbers
MDL Number MFCD15071758
thermostat Physical Properties
Boiling Point 311.2±11.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.056±0.06 g/cm3(Predicted)
Storage room temperature

description Product Description

This compound is primarily utilized in organic synthesis as a versatile intermediate. It plays a significant role in the preparation of various pharmaceutical agents, particularly in the development of pyrrolidine-based compounds. Its structure is often exploited in the synthesis of bioactive molecules, including potential drug candidates targeting neurological and inflammatory disorders. Additionally, it serves as a protective group for amines in peptide synthesis, enabling selective reactions in complex molecular constructions. Its stability and reactivity make it a valuable tool in medicinal chemistry and drug discovery processes.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,800.00
inventory 250mg
10-20 days ฿18,900.00
inventory 1g
10-20 days ฿37,800.00

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Tert-Butyl 3,3-Dimethyl-2-Oxopyrrolidine-1-Carboxylate
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This compound is primarily utilized in organic synthesis as a versatile intermediate. It plays a significant role in the preparation of various pharmaceutical agents, particularly in the development of pyrrolidine-based compounds. Its structure is often exploited in the synthesis of bioactive molecules, including potential drug candidates targeting neurological and inflammatory disorders. Additionally, it serves as a protective group for amines in peptide synthesis, enabling selective reactions in comple

This compound is primarily utilized in organic synthesis as a versatile intermediate. It plays a significant role in the preparation of various pharmaceutical agents, particularly in the development of pyrrolidine-based compounds. Its structure is often exploited in the synthesis of bioactive molecules, including potential drug candidates targeting neurological and inflammatory disorders. Additionally, it serves as a protective group for amines in peptide synthesis, enabling selective reactions in complex molecular constructions. Its stability and reactivity make it a valuable tool in medicinal chemistry and drug discovery processes.

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