(S)-tert-Butyl 4-(4-(4-(2-amino-3-methoxy-3-oxopropyl)phenoxy)butyl)piperidine-1-carboxylate

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Reagent Code: #236479
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CAS Number 142373-57-7

science Other reagents with same CAS 142373-57-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 434.57 g/mol
Formula C₂₄H₃₈N₂O₅
badge Registry Numbers
MDL Number MFCD30533139
inventory_2 Storage & Handling
Storage -20°C, dry, away from light

description Product Description

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure supports selective binding to specific enzyme active sites, enhancing drug efficacy. Commonly employed in research settings to construct complex molecules requiring chiral piperidine motifs. Also utilized in the preparation of proteolysis-targeting chimeras (PROTACs) due to its ability to link targeting ligands with E3 ligase binders. Suitable for conjugation in bioconjugation strategies and medicinal chemistry optimization.

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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 50mg
10-20 days ฿4,370.00
inventory 100mg
10-20 days ฿6,640.00
inventory 250mg
10-20 days ฿9,940.00

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(S)-tert-Butyl 4-(4-(4-(2-amino-3-methoxy-3-oxopropyl)phenoxy)butyl)piperidine-1-carboxylate
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Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure supports selective binding to specific enzyme active sites, enhancing drug efficacy. Commonly employed in research settings to construct complex molecules requiring chiral piperidine motifs. Also utilized in the preparation of proteolysis-targeting chimeras (PROTACs) due to its ability to link targeting ligands with E3 ligase binders. Suit

Used as an intermediate in the synthesis of pharmaceutical compounds, particularly in the development of kinase inhibitors for targeted cancer therapies. Its structure supports selective binding to specific enzyme active sites, enhancing drug efficacy. Commonly employed in research settings to construct complex molecules requiring chiral piperidine motifs. Also utilized in the preparation of proteolysis-targeting chimeras (PROTACs) due to its ability to link targeting ligands with E3 ligase binders. Suitable for conjugation in bioconjugation strategies and medicinal chemistry optimization.

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