DI-TERT-BUTYL ACETYLENEDICARBOXYLATE

98%

Reagent Code: #176645
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CAS Number 66086-33-7

science Other reagents with same CAS 66086-33-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 226.27 g/mol
Formula C₁₂H₁₈O₄
badge Registry Numbers
MDL Number MFCD00008808
thermostat Physical Properties
Melting Point 33-37 °C(lit.)
Boiling Point 80-82 °C0.05 mm Hg(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key reagent in organic synthesis, particularly in Diels-Alder reactions, where it acts as a highly reactive dienophile due to the electron-withdrawing ester groups adjacent to the alkyne. It enables the construction of six-membered rings in cycloaddition processes, useful in the synthesis of complex natural products and pharmaceuticals. Also employed in click chemistry and metal-catalyzed coupling reactions to form functionalized alkenes and heterocycles. Its stability and reactivity profile make it valuable for introducing alkyne functionality in a controlled manner.

Available Sizes & Pricing

Size Availability Unit Price Quantity
250mg
10-20 days ฿2,810.00
1g
10-20 days ฿7,550.00
5g
10-20 days ฿26,440.00
DI-TERT-BUTYL ACETYLENEDICARBOXYLATE
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Used as a key reagent in organic synthesis, particularly in Diels-Alder reactions, where it acts as a highly reactive dienophile due to the electron-withdrawing ester groups adjacent to the alkyne. It enables the construction of six-membered rings in cycloaddition processes, useful in the synthesis of complex natural products and pharmaceuticals. Also employed in click chemistry and metal-catalyzed coupling reactions to form functionalized alkenes and heterocycles. Its stability and reactivity profile ma

Used as a key reagent in organic synthesis, particularly in Diels-Alder reactions, where it acts as a highly reactive dienophile due to the electron-withdrawing ester groups adjacent to the alkyne. It enables the construction of six-membered rings in cycloaddition processes, useful in the synthesis of complex natural products and pharmaceuticals. Also employed in click chemistry and metal-catalyzed coupling reactions to form functionalized alkenes and heterocycles. Its stability and reactivity profile make it valuable for introducing alkyne functionality in a controlled manner.

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