Triisopropyl[(trimethylsilyl)ethynyl]silane
≥97%
- Product Code: 88300
CAS:
107474-02-2
Molecular Weight: | 254.56 g./mol | Molecular Formula: | C₁₄H₃₀Si₂ |
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EC Number: | 811-132-0 | MDL Number: | MFCD28975120 |
Melting Point: | Boiling Point: | 57°C/0.25mmHg(lit.) | |
Density: | 0.81 g/ml | Storage Condition: | 2-8℃, inert gas, dry, sealed |
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.
Product Specification:
Test | Specification |
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APPEARANCE | Colorless to Almost colorless clear liquid |
PURITY | 97-100 |
Infrared spectrum | Conforms to Structure |
Sizes / Availability / Pricing:
Size (g) | Availability | Price | Quantity |
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1.000 | 10-20 days | ฿4,280.00 |
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5.000 | 10-20 days | ฿14,380.00 |
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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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