Date published: 2026-2-7

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4,4,5,5-Tetramethyl-2-(4-methyl-3-nitrophenyl)-1,3,2-dioxaborolane (CAS 1072945-06-2)

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Alternate Names:
4-Methyl-3-nitrophenylboronic acid pinacol ester
CAS Number:
1072945-06-2
Molecular Weight:
263.1
Molecular Formula:
C13H18BNO4
For Research Use Only. Not Intended for Diagnostic or Therapeutic Use.
* Refer to Certificate of Analysis for lot specific data.

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4,4,5,5-Tetramethyl-2-(4-methyl-3-nitrophenyl)-1,3,2-dioxaborolane, a colorless crystalline entity, has low vapor pressure and is soluble in organic solvents like ethanol, acetone, and benzene. Acting as a Lewis acid, 4,4,5,5-Tetramethyl-2-(4-methyl-3-nitrophenyl)-1,3,2-dioxaborolane serves as a proficient catalyst in numerous organic reactions, illustrating its versatile applications in both scientific studies and industrial processes. It is extensively used in catalyzing organic transformations, including Suzuki coupling, Sonogashira coupling, and oxidative coupling. 4,4,5,5-Tetramethyl-2-(4-methyl-3-nitrophenyl)-1,3,2-dioxaborolane applications extends into diverse domains such as material science, photochemistry, and electrochemistry.


4,4,5,5-Tetramethyl-2-(4-methyl-3-nitrophenyl)-1,3,2-dioxaborolane (CAS 1072945-06-2) References

  1. Synthesis of trimethylstannyl arylboronate compounds by Sandmeyer-type transformations and their applications in chemoselective cross-coupling reactions.  |  Qiu, D., et al. 2014. J Org Chem. 79: 1979-88. PMID: 24521293

Ordering Information

Product NameCatalog #UNITPriceQtyFAVORITES

4,4,5,5-Tetramethyl-2-(4-methyl-3-nitrophenyl)-1,3,2-dioxaborolane, 1 g

sc-311067
1 g
$80.00

4,4,5,5-Tetramethyl-2-(4-methyl-3-nitrophenyl)-1,3,2-dioxaborolane, 5 g

sc-311067A
5 g
$320.00