Ethyl 2-((tert-butoxycarbonyl)amino)-2-(pyridin-2-yl)acetate

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Reagent Code: #41175
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CAS Number 313490-90-3

science Other reagents with same CAS 313490-90-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 280.32 g/mol
Formula C₁₄H₂₀N₂O₄
badge Registry Numbers
MDL Number MFCD18249963
thermostat Physical Properties
Boiling Point 405.9±40.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage room temperature, stored under inert gas

description Product Description

This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of complex molecules, particularly in pharmaceutical research. It serves as a building block in the synthesis of various biologically active compounds, including potential drug candidates. The presence of the tert-butoxycarbonyl (Boc) protecting group allows for selective reactions at other functional sites, making it valuable in multi-step synthetic processes. Additionally, its pyridine moiety can contribute to the development of compounds with specific binding properties, often explored in medicinal chemistry for targeting enzymes or receptors. Its application extends to the development of agrochemicals and fine chemicals, where precise structural modifications are required.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿21,879.00
inventory 250mg
10-20 days ฿10,935.00

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Ethyl 2-((tert-butoxycarbonyl)amino)-2-(pyridin-2-yl)acetate
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This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of complex molecules, particularly in pharmaceutical research. It serves as a building block in the synthesis of various biologically active compounds, including potential drug candidates. The presence of the tert-butoxycarbonyl (Boc) protecting group allows for selective reactions at other functional sites, making it valuable in multi-step synthetic processes. Additionally, its pyridine moiety can contribu

This compound is primarily utilized in organic synthesis as a key intermediate for the preparation of complex molecules, particularly in pharmaceutical research. It serves as a building block in the synthesis of various biologically active compounds, including potential drug candidates. The presence of the tert-butoxycarbonyl (Boc) protecting group allows for selective reactions at other functional sites, making it valuable in multi-step synthetic processes. Additionally, its pyridine moiety can contribute to the development of compounds with specific binding properties, often explored in medicinal chemistry for targeting enzymes or receptors. Its application extends to the development of agrochemicals and fine chemicals, where precise structural modifications are required.

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