3,4-Dimethoxybenzeneboronic acid, 98%
3,4-Dimethoxybenzeneboronic acid, 98%
3,4-Dimethoxybenzeneboronic acid, 98%
Thermo Scientific Chemicals

3,4-Dimethoxybenzeneboronic acid, 98%

CAS: 122775-35-3 | C8H11BO4 | 181.98 g/mol
Have Questions?
Change viewbuttonViewtableView
Quantity:
1 g
5 g
25 g
Catalog number B24240.03
also known as B24240-03
Price (TWD)
-
Quantity:
1 g
Request bulk or custom format
Specifications
Beilstein5334877
CAS122775-35-3
Chemical Name or Material3,4-Dimethoxybenzeneboronic acid
Formula Weight181.98
Health Hazard 1H315-H319-H335
View more
3,4-Dimethoxybenzeneboronic acid is used in organic light-emitting diode. It is an important raw material and intermediate used in organic synthesis, pharmaceuticals agrochemicals and dyestuff fields.

This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Scientific Chemicals.

Applications
3,4-Dimethoxybenzeneboronic acid is used in organic light-emitting diode. It is an important raw material and intermediate used in organic synthesis, pharmaceuticals agrochemicals and dyestuff fields.

Solubility
Soluble in water (25 g/L).

Notes
Keep container tightly closed. Store in cool dry conditions in well sealed containers. Incompatible with oxidizing agents.
RUO – Research Use Only

General References:

  1. Ali Raoof.; Paul Depledge.; Niall M. Hamilton.; Nicola S. Hamilton.; James R. Hitchin.; Gemma V. Hopkins.; Allan M. Jordan.; Laura A. Maguire.; Alison E. McGonagle.; Daniel P. Mould.; Mathew Rushbrook.; Helen F. Small.; Kate M. Smith.; Graeme J. Thomson.; Fabrice Turlais.; Ian D. Waddel.; Bohdan Waszkowycz.; Amanda J. Watso.; Donald J. Ogilvie. Toxoflavins and Deazaflavins as the First Reported Selective Small Molecule Inhibitors of Tyrosyl-DNA Phosphodiesterase II. J. Med. Chem. 2013, 56 (16), 6352-6370.
  2. Suzuki coupling (see Appendix 5) with 1-amino-2-bromonaphthalene derivatives has been used in a versatile synthesis of benzo[c]phenanthridine alkaloids: J. Chem. Soc., Perkin 1, 1647 (1996).