CAS 10365-98-7
:(3-Methoxyphenyl)boronic acid
Description:
(3-Methoxyphenyl)boronic acid, with the CAS number 10365-98-7, is an organoboron compound characterized by the presence of a boronic acid functional group attached to a methoxy-substituted phenyl ring. This compound typically appears as a white to off-white solid and is soluble in polar organic solvents such as methanol and ethanol. It exhibits properties typical of boronic acids, including the ability to form reversible complexes with diols, which makes it valuable in various applications, particularly in organic synthesis and medicinal chemistry. The methoxy group enhances its reactivity and solubility, facilitating its use in Suzuki-Miyaura cross-coupling reactions, a key method for forming carbon-carbon bonds. Additionally, (3-Methoxyphenyl)boronic acid can serve as a building block in the synthesis of pharmaceuticals and agrochemicals. Its reactivity and functional versatility make it an important compound in the field of organic chemistry. Safety precautions should be observed when handling this substance, as with all boronic acids, due to potential irritant properties.
Formula:C7H9BO3
InChI:InChI=1S/C7H9BO3/c1-11-7-4-2-3-6(5-7)8(9)10/h2-5,9-10H,1H3
InChI key:InChIKey=NLLGFYPSWCMUIV-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC(OC)=CC=C1
Synonyms:- (3-Methoxyphenyl)boronic acid
- (m-Methoxyphenyl)boronic acid
- 3-Methoxybenzeneboronic acid
- B-(3-Methoxyphenyl)boronic acid
- Benzeneboronic acid, m-methoxy-
- Boronic acid, (3-methoxyphenyl)-
- Boronic acid, B-(3-methoxyphenyl)-
- m-Anisylboronic acid
- m-Methoxybenzeneboronic acid
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Found 8 products.
3-Methoxybenzeneboronic acid, 97%
CAS:<p>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 Sci</p>Formula:C7H9BO3Purity:97%Color and Shape:White to pale cream to pale gray, Crystals or powder or crystalline powderMolecular weight:151.963-Methoxyphenylboronic acid
CAS:Formula:C7H9BO3Purity:96%Color and Shape:SolidMolecular weight:151.95563-Methoxybenzeneboronic acid
CAS:3-Methoxybenzeneboronic acidFormula:C7H9BO3Purity:97%Color and Shape: white to off-white solidMolecular weight:151.96g/mol3-Methoxyphenylboronic Acid (contains varying amounts of Anhydride)
CAS:Formula:C7H9BO3Color and Shape:White to Light yellow to Dark green powder to crystalMolecular weight:151.963-Methoxybenzeneboronic acid
CAS:Formula:C7H9BO3Purity:96%Color and Shape:SolidMolecular weight:151.963-Methoxylphenylboronic Acid (contains varying amounts of Anhydride)
CAS:Controlled Product<p>Applications 3-Methoxyphenylboronic Acid is a phenylboronic acid used to investigate boron function in plants.<br>References Baldwin, T., et al.: Plant Physiol., 103, 115 (1993), Andeme-Onzighi, C., et al.: Planta, 215, 949 (2002), Brown, P., et al.: Plant Biol. 4, 205 (2005),<br></p>Formula:C7H9BO3Color and Shape:WhiteMolecular weight:151.963-Methoxyphenylboronic acid
CAS:<p>3-Methoxyphenylboronic acid is a photophysical molecule that can be used as an analytical reagent in plant physiology and analytical chemistry. 3-Methoxyphenylboronic acid reacts reversibly with copper ions to form a complex. The binding constants of the copper complex depend on the pH of the solution, which can be altered by adding a phosphate derivative to the solution. This reaction was investigated using cross-coupling techniques and showed that the binding constants for this complex are dependent on the type of solvent used. 3-Methoxyphenylboronic acid has also been used to measure glucose levels in blood samples.</p>Formula:C7H9BO3Purity:Min. 95%Color and Shape:White PowderMolecular weight:151.96 g/mol
