3-(tert-Butoxy)-3-oxo-2-(quinolin-4-ylmethyl)propanoic acid

≥95%

Reagent Code: #117525
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CAS Number 1799439-14-7

science Other reagents with same CAS 1799439-14-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 301.34 g/mol
Formula C₁₇H₁₉NO₄
badge Registry Numbers
MDL Number MFCD28098467
thermostat Physical Properties
Boiling Point 471.9±35.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, dry and sealed

description Product Description

This chemical is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of bioactive compounds, particularly those targeting specific enzymes or receptors. Its structure, featuring a quinoline moiety, makes it valuable in the design of molecules with potential therapeutic applications, such as anti-inflammatory or anticancer agents. Additionally, it can be employed in the preparation of complex organic molecules for drug discovery and medicinal chemistry studies. Its tert-butoxy group also provides stability and reactivity, making it suitable for controlled chemical transformations in synthetic pathways.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,290.00
inventory 250mg
10-20 days ฿14,589.00

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3-(tert-Butoxy)-3-oxo-2-(quinolin-4-ylmethyl)propanoic acid
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This chemical is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of bioactive compounds, particularly those targeting specific enzymes or receptors. Its structure, featuring a quinoline moiety, makes it valuable in the design of molecules with potential therapeutic applications, such as anti-inflammatory or anticancer agents. Additionally, it can be employed in the preparation of complex organic molecules for drug discovery and medic

This chemical is primarily utilized in organic synthesis and pharmaceutical research. It serves as a key intermediate in the development of bioactive compounds, particularly those targeting specific enzymes or receptors. Its structure, featuring a quinoline moiety, makes it valuable in the design of molecules with potential therapeutic applications, such as anti-inflammatory or anticancer agents. Additionally, it can be employed in the preparation of complex organic molecules for drug discovery and medicinal chemistry studies. Its tert-butoxy group also provides stability and reactivity, making it suitable for controlled chemical transformations in synthetic pathways.

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