tert-Butyl2-(prop-2-yn-1-yloxy)acetate

98%

Reagent Code: #155143
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CAS Number 339531-55-4

science Other reagents with same CAS 339531-55-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 170.21 g/mol
Formula C₉H₁₄O₃
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of complex molecules through click chemistry. Its alkyne functionality enables efficient copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions, making it valuable in pharmaceutical research and development of bioactive compounds. The tert-butyl ester group provides stability and can be easily deprotected under mild acidic conditions, allowing for selective modification in multi-step syntheses. Commonly employed in the construction of peptidomimetics, agrochemicals, and functionalized polymers.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,450.00
inventory 250mg
10-20 days ฿3,570.00
inventory 1g
10-20 days ฿9,590.00
inventory 5g
10-20 days ฿47,950.00
inventory 10g
10-20 days ฿83,370.00

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tert-Butyl2-(prop-2-yn-1-yloxy)acetate
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Used as a key intermediate in organic synthesis, particularly in the preparation of complex molecules through click chemistry. Its alkyne functionality enables efficient copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions, making it valuable in pharmaceutical research and development of bioactive compounds. The tert-butyl ester group provides stability and can be easily deprotected under mild acidic conditions, allowing for selective modification in multi-step syntheses. Commonly employed in th

Used as a key intermediate in organic synthesis, particularly in the preparation of complex molecules through click chemistry. Its alkyne functionality enables efficient copper-catalyzed azide-alkyne cycloaddition (CuAAC) reactions, making it valuable in pharmaceutical research and development of bioactive compounds. The tert-butyl ester group provides stability and can be easily deprotected under mild acidic conditions, allowing for selective modification in multi-step syntheses. Commonly employed in the construction of peptidomimetics, agrochemicals, and functionalized polymers.

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