BOC-4-OXO-L-PROLINE TERT-BUTYL ESTER

97%

Reagent Code: #144368
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CAS Number 166410-05-5

science Other reagents with same CAS 166410-05-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.34 g/mol
Formula C₁₄H₂₃NO₅
badge Registry Numbers
MDL Number MFCD06797013
inventory_2 Storage & Handling
Storage 2~8℃

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its protected functional groups allow selective reactions in multi-step organic syntheses, especially in peptide and peptidomimetic construction. The tert-butyl ester and BOC-protected amine provide stability and solubility in organic solvents, making it suitable for solid-phase and solution-phase peptide synthesis. Commonly employed in medicinal chemistry for building complex heterocyclic structures with controlled stereochemistry.

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Test Parameter Specification
Appearance Solid
Purity (%) 96.5-100%
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿159.50
inventory 1g
10-20 days ฿165.00
inventory 5g
10-20 days ฿700.00
inventory 25g
10-20 days ฿3,350.00

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BOC-4-OXO-L-PROLINE TERT-BUTYL ESTER
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its protected functional groups allow selective reactions in multi-step organic syntheses, especially in peptide and peptidomimetic construction. The tert-butyl ester and BOC-protected amine provide stability and solubility in organic solvents, making it suitable for solid-phase and solution-phase peptide synthesis. Commonly employed in m

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of protease inhibitors and other biologically active molecules. Its protected functional groups allow selective reactions in multi-step organic syntheses, especially in peptide and peptidomimetic construction. The tert-butyl ester and BOC-protected amine provide stability and solubility in organic solvents, making it suitable for solid-phase and solution-phase peptide synthesis. Commonly employed in medicinal chemistry for building complex heterocyclic structures with controlled stereochemistry.

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