trimethyl(3-phenylprop-1-yn-1-yl)silane

95%

Reagent Code: #242098
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CAS Number 31683-47-3

science Other reagents with same CAS 31683-47-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.341 g/mol
Formula C₁₂H₁₆Si
badge Registry Numbers
MDL Number MFCD22574863
thermostat Physical Properties
Boiling Point 228.0±19.0 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a silylating agent in organic synthesis, particularly in the preparation of alkynylsilanes for cross-coupling reactions. It serves as a building block in the development of conjugated molecules for materials science, including organic semiconductors and luminescent compounds. Its alkyne functionality allows participation in click chemistry and palladium-catalyzed coupling reactions, enabling the construction of complex molecular architectures. Also employed in the modification of substrates for chromatographic analysis due to enhanced volatility and thermal stability imparted by the trimethylsilyl group.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿32,000.00
inventory 250mg
10-20 days ฿48,000.00
inventory 500mg
10-20 days ฿72,000.00
inventory 1g
10-20 days ฿96,000.00

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trimethyl(3-phenylprop-1-yn-1-yl)silane
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Used as a silylating agent in organic synthesis, particularly in the preparation of alkynylsilanes for cross-coupling reactions. It serves as a building block in the development of conjugated molecules for materials science, including organic semiconductors and luminescent compounds. Its alkyne functionality allows participation in click chemistry and palladium-catalyzed coupling reactions, enabling the construction of complex molecular architectures. Also employed in the modification of substrates for c

Used as a silylating agent in organic synthesis, particularly in the preparation of alkynylsilanes for cross-coupling reactions. It serves as a building block in the development of conjugated molecules for materials science, including organic semiconductors and luminescent compounds. Its alkyne functionality allows participation in click chemistry and palladium-catalyzed coupling reactions, enabling the construction of complex molecular architectures. Also employed in the modification of substrates for chromatographic analysis due to enhanced volatility and thermal stability imparted by the trimethylsilyl group.

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