3-(Trimethylsilyl)propynal

≥90%(GC)

Reagent Code: #239953
label
Alias 3-Trimethylsilylpropynealdehyde; 3-Trimethylsilylpropynealdehyde
fingerprint
CAS Number 2975-46-4

science Other reagents with same CAS 2975-46-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 126.23 g/mol
Formula C₆H₁₀OSi
badge Registry Numbers
MDL Number MFCD01103709
thermostat Physical Properties
Boiling Point 52 °C
inventory_2 Storage & Handling
Density 0.86
Storage 2~8°C

description Product Description

Used as a key intermediate in organic synthesis, particularly in the preparation of functionalized alkynes and conjugated systems. Its aldehyde group allows for various nucleophilic addition reactions, while the trimethylsilyl-protected alkyne can be deprotected to generate reactive acetylene species for Sonogashira or other coupling reactions. Commonly employed in the synthesis of natural products, pharmaceuticals, and advanced materials where controlled alkyne reactivity is required. Its stability and selective reactivity make it valuable in multi-step synthetic routes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿159.50
inventory 1g
10-20 days ฿580.00
inventory 25g
10-20 days ฿8,020.00
inventory 5g
10-20 days ฿1,800.00
3-(Trimethylsilyl)propynal
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Used as a key intermediate in organic synthesis, particularly in the preparation of functionalized alkynes and conjugated systems. Its aldehyde group allows for various nucleophilic addition reactions, while the trimethylsilyl-protected alkyne can be deprotected to generate reactive acetylene species for Sonogashira or other coupling reactions. Commonly employed in the synthesis of natural products, pharmaceuticals, and advanced materials where controlled alkyne reactivity is required. Its stability and

Used as a key intermediate in organic synthesis, particularly in the preparation of functionalized alkynes and conjugated systems. Its aldehyde group allows for various nucleophilic addition reactions, while the trimethylsilyl-protected alkyne can be deprotected to generate reactive acetylene species for Sonogashira or other coupling reactions. Commonly employed in the synthesis of natural products, pharmaceuticals, and advanced materials where controlled alkyne reactivity is required. Its stability and selective reactivity make it valuable in multi-step synthetic routes.

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