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62108-37-6

1-(Trimethylsilyl)-1-butyne

Catalog#: AR0039A5  |   CAS#: 62108-37-6  |   MDL#: MFCD19707267  |   MF: C7H14Si  |   MW: 126.2716

Packsize Purity Price Availability Quantity
250mg 95% $6.00 Global Stock Buy Now Add To Cart
1g 95% $7.00 Global Stock Buy Now Add To Cart
5g 95% $23.00 Global Stock Buy Now Add To Cart
10g 95% $44.00 Global Stock Buy Now Add To Cart
25g 95% $87.00 Global Stock Buy Now Add To Cart
100g 95% $260.00 Global Stock Buy Now Add To Cart
500g 95% $1,039.00 Global Stock Buy Now Add To Cart
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Catalog Number AR0039A5
Chemical Name 1-(Trimethylsilyl)-1-butyne
CAS Number 62108-37-6
Molecular Formula C7H14Si
Molecular Weight 126.2716
MDL Number MFCD19707267
SMILES CCC#C[Si](C)(C)C

1-(Trimethylsilyl)-1-butyne, commonly known as TMSC≡CH, is a versatile compound widely used in organic synthesis as a building block for the construction of various organic molecules. This compound serves as a valuable tool in the creation of complex carbon frameworks due to its unique reactivity and functional group compatibility.In chemical synthesis, TMSC≡CH is frequently employed as a precursor in Sonogashira cross-coupling reactions, which are essential transformations for the formation of carbon-carbon bonds. By reacting TMSC≡CH with aryl or vinyl halides in the presence of a palladium catalyst and a base, new carbon-carbon bonds can be selectively formed, allowing for the preparation of a wide range of alkynes and polyynes.Additionally, TMSC≡CH can participate in various other reactions such as nucleophilic additions, cycloadditions, and hydrogenation, making it a versatile tool for the synthesis of diverse organic compounds. The trimethylsilyl group provides stability and can be easily removed under mild conditions to reveal the terminal alkyne functionality, further expanding the synthetic possibilities of TMSC≡CH in chemical transformations.Overall, the application of 1-(Trimethylsilyl)-1-butyne in chemical synthesis offers chemists a valuable building block for the development of new molecules with unique properties and structures. By leveraging its reactivity and compatibility with various reaction conditions, TMSC≡CH plays a crucial role in the design and synthesis of complex organic compounds in modern organic chemistry practices.
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GHS Pictogram
Signal Word Danger
UN# 1993
Hazard Statements H226-H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class 3
Packing Group

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