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99770-93-1

1,4-Benzenediboronic Acid Bis(pinacol) Ester

Catalog#: AR003FVJ  |   CAS#: 99770-93-1  |   MDL#: MFCD08276852  |   MF: C18H28B2O4  |   MW: 330.0345

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250mg 97% $3.00 Global Stock Buy Now Add To Cart
1g 97% $3.00 Global Stock Buy Now Add To Cart
5g 97% $6.00 Global Stock Buy Now Add To Cart
10g 97% $11.00 Global Stock Buy Now Add To Cart
25g 97% $27.00 Global Stock Buy Now Add To Cart
100g 97% $107.00 Global Stock Buy Now Add To Cart
500g 97% $488.00 Global Stock Buy Now Add To Cart
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Catalog Number AR003FVJ
Chemical Name 1,4-Benzenediboronic Acid Bis(pinacol) Ester
CAS Number 99770-93-1
Molecular Formula C18H28B2O4
Molecular Weight 330.0345
MDL Number MFCD08276852
SMILES CC1(C)OB(OC1(C)C)c1ccc(cc1)B1OC(C(O1)(C)C)(C)C

1,4-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene is a versatile compound commonly used in chemical synthesis as a key building block for the creation of complex organic molecules. This compound serves as a valuable reagent in Suzuki-Miyaura cross-coupling reactions, a widely employed method in organic synthesis for forming carbon-carbon bonds. Due to its boron-containing structure, 1,4-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene offers a unique electronic and steric environment that facilitates its participation in diverse coupling reactions with aryl halides or pseudohalides. By using this compound as a coupling partner, chemists can efficiently access a wide range of functionalized biaryl compounds, which are prevalent motifs in pharmaceuticals, agrochemicals, and materials science. Moreover, the exceptional stability and compatibility of 1,4-Bis(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzene make it a valuable tool for the construction of complex molecular architectures in the synthesis of new drugs, materials, and fine chemicals.
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GHS Pictogram
Signal Word Warning
UN# N/A
Hazard Statements H315-H319-H335
Precautionary Statements P261-P305+P351+P338
Class N/A
Packing Group N/A

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