tert-butyl 3-(2-diazoacetyl)piperidine-1-carboxylate

95%

Reagent Code: #239022
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CAS Number 1796553-29-1

science Other reagents with same CAS 1796553-29-1

blur_circular Chemical Specifications

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Weight 253.302 g/mol
Formula C₁₂H₁₉N₃O₃
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of enzyme inhibitors and bioactive molecules. Its diazo group enables participation in cycloaddition and insertion reactions, making it valuable in constructing complex heterocyclic systems. Commonly employed in medicinal chemistry for scaffold diversification and in the preparation of peptidomimetics. Also utilized in catalysis studies involving transition metals, where the diazo functionality acts as a carbene precursor for C–H functionalization reactions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,240.00
inventory 250mg
10-20 days ฿20,440.00
inventory 1g
10-20 days ฿61,450.00

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tert-butyl 3-(2-diazoacetyl)piperidine-1-carboxylate
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Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of enzyme inhibitors and bioactive molecules. Its diazo group enables participation in cycloaddition and insertion reactions, making it valuable in constructing complex heterocyclic systems. Commonly employed in medicinal chemistry for scaffold diversification and in the preparation of peptidomimetics. Also utilized in catalysis studies involving transition metals, where the diazo functionality acts a

Used as a key intermediate in the synthesis of pharmaceutical compounds, particularly in the development of enzyme inhibitors and bioactive molecules. Its diazo group enables participation in cycloaddition and insertion reactions, making it valuable in constructing complex heterocyclic systems. Commonly employed in medicinal chemistry for scaffold diversification and in the preparation of peptidomimetics. Also utilized in catalysis studies involving transition metals, where the diazo functionality acts as a carbene precursor for C–H functionalization reactions.

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