Triisopropyl[(trimethylsilyl)ethynyl]silane
≥97%
Reagent
Code: #88300
CAS Number
107474-02-2
blur_circular Chemical Specifications
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Molecular Information
Weight
254.56 g/mol
Formula
C₁₄H₃₀Si₂
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Registry Numbers
EC Number
811-132-0
MDL Number
MFCD28975120
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Physical Properties
Boiling Point
57°C/0.25mmHg(lit.)
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Storage & Handling
Density
0.81 g/ml
Storage
2-8℃, inert gas, dry, sealed
description Product Description
This chemical is primarily used in organic synthesis as a versatile reagent for introducing silyl-protected alkynes into various molecular structures. It is particularly valuable in cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds, enabling the construction of complex organic frameworks. Its stability and reactivity make it a useful tool in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of silicon-containing polymers and as a precursor in the preparation of specialized silicon-based compounds. Its ability to act as a protecting group for alkynes further enhances its utility in multi-step synthetic processes.
format_list_bulleted Product Specification
Test Parameter | Specification |
---|---|
Appearance | Colorless to almost colorless clear liquid |
Purity | 97-100 |
Infrared Spectrum | Conforms to Structure |
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Triisopropyl[(trimethylsilyl)ethynyl]silane
This chemical is primarily used in organic synthesis as a versatile reagent for introducing silyl-protected alkynes into various molecular structures. It is particularly valuable in cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds, enabling the construction of complex organic frameworks. Its stability and reactivity make it a useful tool in the development of pharmaceuticals, agrochemicals, and advanced materials. Additionally, it is employed in the synthesis of silicon-containing polymers and as a precursor in the preparation of specialized silicon-based compounds. Its ability to act as a protecting group for alkynes further enhances its utility in multi-step synthetic processes.
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