CAS 5720-07-0
:4-Methoxyphenylboronic acid
Description:
4-Methoxyphenylboronic acid, with the CAS number 5720-07-0, 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 is known for its ability to form reversible covalent bonds with diols, making it useful in various applications, including organic synthesis and as a reagent in Suzuki coupling reactions, which are pivotal in the formation of carbon-carbon bonds. The methoxy group enhances the electron density of the aromatic ring, influencing its reactivity and stability. Additionally, 4-methoxyphenylboronic acid can serve as a building block in the synthesis of pharmaceuticals and agrochemicals. Its boronic acid functionality allows for the formation of complexes with biomolecules, which has implications in medicinal chemistry and materials science. Proper handling and storage are essential due to its reactivity and potential environmental impact.
Formula:C7H9BO3
InChI:InChI=1S/C7H9BO3/c1-11-7-4-2-6(3-5-7)8(9)10/h2-5,9-10H,1H3
InChI key:InChIKey=VOAAEKKFGLPLLU-UHFFFAOYSA-N
SMILES:B(O)(O)C1=CC=C(OC)C=C1
Synonyms:- (4-Methoxyphenyl)Borane
- (4-Methoxyphenyl)boronic acid
- (p-Methoxyphenyl)boronic acid
- 4-Anisylboronic acid
- 4-Methoxybenzeneboronic Acid
- 4-Methoxylphenylboronic acid
- B-(4-Methoxyphenyl)boronic acid
- Benzeneboronic acid, p-methoxy-
- Boronic acid, (4-methoxyphenyl)-
- Boronic acid, B-(4-methoxyphenyl)-
- [4-(Methyloxy)phenyl]boronic acid
- p-Anisylboronic acid
- p-Methoxybenzeneboronic acid
- p-Methoxyphenylboronic
- AKOS 91312
- AKOS BRN-0016
- P-METHOXYPHENYLBORONIC ACID
- RARECHEM AH PB 0191
- BIO-FARMA BF000847
- 4-METHOXYPHENYLBORONIC ACID
- 5-Methoxybenzeneboronic acid
- 4-METHOXYPHENYLBORONIC AICD
- 4-METHOXYPHENYL BORONIC ACID, 4-METHOXYBENZENEBORONIC ACID, P-ANISYLBORONIC ACID(4)
- TIMTEC-BB SBB004055
- 4-boronoanisole
- p-methoxy-benzeneboronicaci
- (4-methoxyphenyl)-boronicaci
- 4-Methoxybenzeneboronicacid,98%
- p-methoxyphenyl-boronicaci
- See more synonyms
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Found 9 products.
4-Methoxyphenylboronic Acid (contains varying amounts of Anhydride)
CAS:Formula:C7H9BO3Purity:97.0 to 113.0 %Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:151.964-Methoxybenzeneboronic acid, 97+%
CAS:<p>4-Methoxybenzeneboronic acid is used for Suzuki-Miyaura cross-coupling reactions, Pd-catalyzed direct arylation, Highly effective synthesis using palladium-catalyzed arylation Suzuki-Miyaura cross-coupling in water, Palladium-catalyzed stereoselective Heck-type reaction, Tandem-type Pd(II)-catalyzed</p>Formula:C7H9BO3Purity:97+%Color and Shape:White to pale cream to pale brown, Crystals or powder or crystalline powderMolecular weight:151.964-Methoxybenzeneboronic acid
CAS:Formula:C7H9BO3Purity:98%Color and Shape:SolidMolecular weight:151.95564-Methoxybenzeneboronic acid
CAS:<p>4-Methoxybenzeneboronic acid</p>Formula:C7H9BO3Purity:≥95%Color and Shape: white crystalline powderMolecular weight:151.95556g/mol4-Methoxybenzeneboronic acid
CAS:Formula:C7H9BO3Purity:97.0%Color and Shape:White chrystalline solidMolecular weight:151.964-Methoxyphenylboronic Acid extrapure, 98%
CAS:Formula:C7H9BO3Purity:min. 98%Color and Shape:White to Off-white, Crystalline powderMolecular weight:151.94-Methoxylphenylboronic Acid
CAS:Controlled Product<p>Applications 4-Methoxylphenylboronic 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:151.964-Methoxyphenyl boronic acid
CAS:<p>4-Methoxyphenyl boronic acid is a molecule with a hydroxyl group and a boronic acid. It is synthesized by reacting biphenyl with trifluoroacetic acid in the presence of sodium carbonate and palladium-catalyzed coupling. 4-Methoxyphenyl boronic acid has shown to bind to the receptor for fatty acids, which may be due to its structural similarity to p-hydroxybenzoic acid. The protonated form of this molecule has been shown to react with an electrophilic carbon atom and an electron-deficient alkyl or vinyl halide, resulting in ring formation. This reaction is known as the Suzuki coupling reaction.</p>Formula:C7H9BO3Purity:Min. 95%Color and Shape:PowderMolecular weight:151.96 g/mol








