3-(Trimethylsilyl)propynoic acid

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Reagent Code: #239799
label
Alias 3-(trimethylsilyl)propyne acid
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CAS Number 5683-31-8

science Other reagents with same CAS 5683-31-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 142.23 g/mol
Formula C₆H₁₀O₂Si
badge Registry Numbers
MDL Number MFCD00190216
thermostat Physical Properties
Melting Point 47-49 °C(lit.)
Boiling Point 105-110 °C10 mm Hg(lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key reagent in organic synthesis, particularly in Sonogashira coupling reactions, where it introduces a trimethylsilyl-protected alkyne group. This allows for the controlled formation of carbon–carbon bonds in the construction of complex molecules, including pharmaceuticals and advanced materials. The trimethylsilyl (TMS) group acts as a protecting group that can be easily removed under mild conditions, enabling further functionalization downstream. It is especially valuable in the synthesis of conjugated enynes and alkynoic derivatives used in medicinal chemistry and materials science. Its stability and reactivity profile make it suitable for multi-step synthetic sequences.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿176.00
inventory 250mg
10-20 days ฿187.00

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3-(Trimethylsilyl)propynoic acid
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Used as a key reagent in organic synthesis, particularly in Sonogashira coupling reactions, where it introduces a trimethylsilyl-protected alkyne group. This allows for the controlled formation of carbon–carbon bonds in the construction of complex molecules, including pharmaceuticals and advanced materials. The trimethylsilyl (TMS) group acts as a protecting group that can be easily removed under mild conditions, enabling further functionalization downstream. It is especially valuable in the synthesis of

Used as a key reagent in organic synthesis, particularly in Sonogashira coupling reactions, where it introduces a trimethylsilyl-protected alkyne group. This allows for the controlled formation of carbon–carbon bonds in the construction of complex molecules, including pharmaceuticals and advanced materials. The trimethylsilyl (TMS) group acts as a protecting group that can be easily removed under mild conditions, enabling further functionalization downstream. It is especially valuable in the synthesis of conjugated enynes and alkynoic derivatives used in medicinal chemistry and materials science. Its stability and reactivity profile make it suitable for multi-step synthetic sequences.

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