Bis(trimethylsilyl)acetylene

98%

Reagent Code: #143270
label
Alias Bis(trimethylsilyl)acetylene; Bis(trimethylsilyl)acetylene
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CAS Number 14630-40-1

science Other reagents with same CAS 14630-40-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 170.4 g/mol
Formula C₈H₁₈Si₂
badge Registry Numbers
EC Number 238-671-9
MDL Number MFCD00008276
thermostat Physical Properties
Melting Point 21-24 °C(lit.)
Boiling Point 136-137 °C(lit.)
inventory_2 Storage & Handling
Density 0.752 g/mL at 25 °C(lit.)
Storage 2~8°C

description Product Description

Used as a reagent in organic synthesis, particularly in palladium-catalyzed coupling reactions to introduce acetylene groups. It serves as a protected form of acetylene, enabling controlled alkyne incorporation in complex molecule construction, such as natural products and pharmaceuticals. Commonly applied in Sonogashira coupling where its stability and low reactivity under basic conditions allow selective transformations. Also utilized in materials science for synthesizing conjugated polymers and organosilicon-based functional materials due to its thermal stability and volatility, making it suitable for vapor-phase deposition processes.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 2ml
10-20 days ฿400.00
inventory 10ml
10-20 days ฿720.00
inventory 50ml
10-20 days ฿2,770.00
inventory 250ml
10-20 days ฿11,550.00
Bis(trimethylsilyl)acetylene
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Used as a reagent in organic synthesis, particularly in palladium-catalyzed coupling reactions to introduce acetylene groups. It serves as a protected form of acetylene, enabling controlled alkyne incorporation in complex molecule construction, such as natural products and pharmaceuticals. Commonly applied in Sonogashira coupling where its stability and low reactivity under basic conditions allow selective transformations. Also utilized in materials science for synthesizing conjugated polymers and organo

Used as a reagent in organic synthesis, particularly in palladium-catalyzed coupling reactions to introduce acetylene groups. It serves as a protected form of acetylene, enabling controlled alkyne incorporation in complex molecule construction, such as natural products and pharmaceuticals. Commonly applied in Sonogashira coupling where its stability and low reactivity under basic conditions allow selective transformations. Also utilized in materials science for synthesizing conjugated polymers and organosilicon-based functional materials due to its thermal stability and volatility, making it suitable for vapor-phase deposition processes.

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