(S)-2-((tert-Butoxycarbonyl)amino)-3-(tetrahydro-2H-pyran-4-yl)propanoic acid

≥98%

Reagent Code: #57128
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CAS Number 368866-33-5

science Other reagents with same CAS 368866-33-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 273.33 g/mol
Formula C₁₃H₂₃NO₅
badge Registry Numbers
MDL Number MFCD18252725
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry

description Product Description

This compound is primarily used in the synthesis of peptides and pharmaceutical intermediates. It serves as a key building block in the development of biologically active molecules, particularly in drug discovery and medicinal chemistry. The tert-butoxycarbonyl (Boc) group provides protection for the amino group during chemical reactions, ensuring selective modification of other functional groups. Its tetrahydro-2H-pyran-4-yl moiety contributes to the compound's structural diversity, making it valuable in designing molecules with specific binding properties or therapeutic effects. It is often employed in the preparation of protease inhibitors, receptor antagonists, and other small-molecule drugs targeting various diseases.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿9,243.00
250mg
10-20 days ฿15,705.00
1g
10-20 days ฿42,462.00
(S)-2-((tert-Butoxycarbonyl)amino)-3-(tetrahydro-2H-pyran-4-yl)propanoic acid
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This compound is primarily used in the synthesis of peptides and pharmaceutical intermediates. It serves as a key building block in the development of biologically active molecules, particularly in drug discovery and medicinal chemistry. The tert-butoxycarbonyl (Boc) group provides protection for the amino group during chemical reactions, ensuring selective modification of other functional groups. Its tetrahydro-2H-pyran-4-yl moiety contributes to the compound's structural diversity, making it valuable i

This compound is primarily used in the synthesis of peptides and pharmaceutical intermediates. It serves as a key building block in the development of biologically active molecules, particularly in drug discovery and medicinal chemistry. The tert-butoxycarbonyl (Boc) group provides protection for the amino group during chemical reactions, ensuring selective modification of other functional groups. Its tetrahydro-2H-pyran-4-yl moiety contributes to the compound's structural diversity, making it valuable in designing molecules with specific binding properties or therapeutic effects. It is often employed in the preparation of protease inhibitors, receptor antagonists, and other small-molecule drugs targeting various diseases.

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