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3,4-Dimethoxybenzeneboronic acid, 98%, Thermo Scientific Chemicals
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Catalog number B24240.14
also known as B24240-14
Price (USD)/ Each
264.00
-
Quantity:
25 g
Price (USD)/ Each
264.00
3,4-Dimethoxybenzeneboronic acid, 98%, Thermo Scientific Chemicals
Catalog numberB24240.14
Price (USD)/ Each
264.00
-
Chemical Identifiers
CAS122775-35-3
IUPAC Name(3,4-dimethoxyphenyl)boronic acid
Molecular FormulaC8H11BO4
InChI KeyRCVDPBFUMYUKPB-UHFFFAOYSA-N
SMILESCOC1=CC=C(C=C1OC)B(O)O
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Specifications
Specification Sheet
Specification SheetProton NMRConforms to structure
FormPowder
Assay (HPLC)≥97.5%
Appearance (Color)Pale cream to cream to pale brown
Assay (Aqueous acid-base Titration)≥97.5%
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.
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:
- 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.
- 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).