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68716-50-7

2-(2,4-Dichlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane

Catalog#: AR003FFH  |   CAS#: 68716-50-7  |   MDL#: MFCD06795660  |   MF: C12H15BCl2O2  |   MW: 272.9633

Packsize Purity Price Availability Quantity
100mg 97% $5.00 Global Stock Buy Now Add To Cart
250mg 97% $5.00 Global Stock Buy Now Add To Cart
1g 97% $14.00 Global Stock Buy Now Add To Cart
5g 97% $61.00 Global Stock Buy Now Add To Cart
10g 97% $111.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003FFH
Chemical Name 2-(2,4-Dichlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane
CAS Number 68716-50-7
Molecular Formula C12H15BCl2O2
Molecular Weight 272.9633
MDL Number MFCD06795660
SMILES Clc1ccc(c(c1)Cl)B1OC(C(O1)(C)C)(C)C

2-(2,4-Dichlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile and valuable chemical compound widely utilized in chemical synthesis processes. This compound serves as a key building block in the synthesis of various organic compounds due to its unique reactivity and functional groups.In chemical synthesis, 2-(2,4-Dichlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is often used as a boron-containing reagent in Suzuki-Miyaura cross-coupling reactions. This reaction is a powerful tool in organic synthesis for forming carbon-carbon bonds efficiently. By reacting with suitable aryl halides or pseudohalides in the presence of a palladium catalyst, this compound can participate in cross-coupling reactions to generate biaryl compounds.Furthermore, the dioxaborolane functionality of this compound enables it to undergo selective and mild transformations in various chemical reactions. It can be employed in the installation of functional groups, the creation of pharmaceutical intermediates, and the modification of complex molecules in a controlled manner.Overall, 2-(2,4-Dichlorophenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane plays a critical role in modern organic synthesis strategies by offering chemists a reliable method to construct intricate molecular structures with high efficiency and selectivity.
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