tert-Butyl 2-methyl-3-oxopyrrolidine-1-carboxylate

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Reagent Code: #151657
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CAS Number 1539946-20-7

science Other reagents with same CAS 1539946-20-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 199.250 g/mol
Formula C₁₀H₁₇NO₃
badge Registry Numbers
MDL Number MFCD22566674
thermostat Physical Properties
Boiling Point 279.9±33.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.086±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its structure supports the construction of complex nitrogen-containing heterocycles, which are common in medicinal chemistry. The compound is valuable in creating peptidomimetics and enzyme inhibitors due to its ability to mimic proline-like scaffolds. It also serves in combinatorial chemistry for generating diverse compound libraries aimed at drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,170.00
inventory 250mg
10-20 days ฿5,760.00
inventory 1g
10-20 days ฿20,320.00
inventory 5g
10-20 days ฿72,210.00

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tert-Butyl 2-methyl-3-oxopyrrolidine-1-carboxylate
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its structure supports the construction of complex nitrogen-containing heterocycles, which are common in medicinal chemistry. The compound is valuable in creating peptidomimetics and enzyme inhibitors due to its ability to mimic proline-like scaffolds. It also serves in combinatorial chemistry for generating diverse compound libraries aimed at drug discovery.

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of bioactive molecules and drug candidates. Its structure supports the construction of complex nitrogen-containing heterocycles, which are common in medicinal chemistry. The compound is valuable in creating peptidomimetics and enzyme inhibitors due to its ability to mimic proline-like scaffolds. It also serves in combinatorial chemistry for generating diverse compound libraries aimed at drug discovery.

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