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4,4,5,5-Tetramethyl-2-(prop-1-en-1-yl)-1,3,2-dioxaborolane

Catalog#: AR003L2E  |   CAS#: 72824-05-6  |   MDL#: MFCD15143598  |   MF: C9H17BO2  |   MW: 168.0411

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5g 95% $952.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003L2E
Chemical Name 4,4,5,5-Tetramethyl-2-(prop-1-en-1-yl)-1,3,2-dioxaborolane
CAS Number 72824-05-6
Molecular Formula C9H17BO2
Molecular Weight 168.0411
MDL Number MFCD15143598
SMILES CC=CB1OC(C(O1)(C)C)(C)C

4,4,5,5-Tetramethyl-2-(prop-1-en-1-yl)-1,3,2-dioxaborolane is a versatile compound commonly used in chemical synthesis. This compound serves as a valuable building block, particularly in organic chemistry, due to its unique structure and reactivity. In particular, it is frequently employed as a boron-containing reagent in various synthetic transformations.One of the key applications of 4,4,5,5-Tetramethyl-2-(prop-1-en-1-yl)-1,3,2-dioxaborolane is in Suzuki-Miyaura cross-coupling reactions. In this widely utilized organic reaction, the compound can act as a boron source to facilitate the formation of carbon-carbon bonds between an aryl or vinyl halide and an organoboron compound. This reaction is pivotal in the synthesis of complex organic molecules, such as pharmaceuticals, agrochemicals, and materials.Furthermore, 4,4,5,5-Tetramethyl-2-(prop-1-en-1-yl)-1,3,2-dioxaborolane is also employed in other types of coupling reactions, such as Heck and Sonogashira reactions, enabling the construction of various carbon-carbon and carbon-heteroatom bonds. Its unique structure and boron functionality make it a valuable reagent for the preparation of diverse organic compounds with high efficiency and selectivity in chemical synthesis.
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GHS Pictogram
Signal Word Warning
UN# -
Hazard Statements H302-H315-H319-H335
Precautionary Statements P280-P305+P351+P338
Class -
Packing Group -

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