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75867-40-2

4-[(Trimethylsilyl)ethynyl]benzonitrile

Catalog#: AR003L9U  |   CAS#: 75867-40-2  |   MDL#: MFCD07784408  |   MF: C12H13NSi  |   MW: 199.3238

Packsize Purity Price Availability Quantity
100mg 97% $17.00 Global Stock Buy Now Add To Cart
250mg 97% $27.00 Global Stock Buy Now Add To Cart
1g 97% $73.00 Global Stock Buy Now Add To Cart
5g 97% $279.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003L9U
Chemical Name 4-[(Trimethylsilyl)ethynyl]benzonitrile
CAS Number 75867-40-2
Molecular Formula C12H13NSi
Molecular Weight 199.3238
MDL Number MFCD07784408
SMILES N#Cc1ccc(cc1)C#C[Si](C)(C)C

4-((Trimethylsilyl)ethynyl)benzonitrile is a versatile compound widely used in chemical synthesis for its unique properties and wide range of applications. This compound is commonly employed as a reagent in organic reactions due to its ability to undergo various transformations, making it a valuable tool for synthetic chemists.One important application of 4-((Trimethylsilyl)ethynyl)benzonitrile is in the synthesis of complex organic molecules through Sonogashira coupling reactions. In this process, the ethynyl group of the compound acts as a reactive site, allowing it to be incorporated into larger molecular structures by forming carbon-carbon bonds with other organic molecules. This reaction is commonly used to introduce alkynyl groups into target compounds, making it a powerful tool for the construction of diverse organic frameworks.Additionally, 4-((Trimethylsilyl)ethynyl)benzonitrile can also serve as a precursor for the synthesis of various heterocyclic compounds, such as pyridines and pyrimidines. By reacting this compound with appropriate reagents, chemists can access a wide range of heterocycles that are essential building blocks in pharmaceuticals, agrochemicals, and materials science.Furthermore, the trimethylsilyl group in 4-((Trimethylsilyl)ethynyl)benzonitrile provides protection for the ethynyl functionality during synthetic manipulations, enabling selective reactions and allowing for the precise control of chemical transformations. This protective group can be selectively removed under mild conditions, facilitating further functionalization of the compound and leading to the construction of complex molecular architectures.Overall, the unique reactivity and versatility of 4-((Trimethylsilyl)ethynyl)benzonitrile make it a valuable reagent in chemical synthesis, enabling the efficient construction of diverse organic molecules with applications in various fields of science and industry.
75867-40-2

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GHS Pictogram
Signal Word Warning
UN# -
Hazard Statements H315-H319-H335-H413
Precautionary Statements P261-P305+P351+P338
Class -
Packing Group -

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