CAS 5720-06-9

2-Methoxyphenylboronic acid

Description:

2-Methoxyphenylboronic acid, with the CAS number 5720-06-9, 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 solvents such as water and alcohols due to the presence of the boronic acid group, which can form hydrogen bonds. It is known for its utility in organic synthesis, particularly in Suzuki-Miyaura cross-coupling reactions, where it serves as a versatile building block for the formation of carbon-carbon bonds. The methoxy group enhances its reactivity and solubility, making it a valuable reagent in medicinal chemistry and materials science. Additionally, 2-methoxyphenylboronic acid can participate in various chemical transformations, including the formation of boronate esters and coordination with metal catalysts. Its ability to form reversible complexes with diols also makes it useful in sensing applications. Overall, this compound is significant in both academic research and industrial applications due to its unique chemical properties.

Formula: C₇H₉BO₃

InChI: InChI=1S/C7H9BO3/c1-11-7-5-3-2-4-6(7)8(9)10/h2-5,9-10H,1H3

InChI key: InChIKey=ROEQGIFOWRQYHD-UHFFFAOYSA-N

SMILES: O(C)C1=C(B(O)O)C=CC=C1

Synonyms:

• (2-Methoxyphenyl)boric acid
• 2-Methoxyphenylboronic acid
• B-(2-Methoxyphenyl)boronic acid
• Benzeneboronic acid, o-methoxy-
• Boronic acid, (2-methoxyphenyl)-
• Boronic acid, B-(2-methoxyphenyl)-
• o-Anisylboronic acid
• o-Methoxybenzeneboronic acid
• o-Methoxyphenylboronic acid

2-Methoxyphenylboronic Acid (contains varying amounts of Anhydride)

CAS: 5720-06-9

Formula: C₇H₉BO₃

Purity: 97.0 to 113.0 %

Color and Shape: White to Almost white powder to crystal

Molecular weight: 151.96

Ref: 3B-M1261

2-Methoxybenzeneboronic acid, 97%

CAS: 5720-06-9

2-Methoxylphenylboronic acid is a phenylboronic acid used to investigate boron function in plants. It is used in Suzuki reaction, organic reaction that is classified as a coupling reaction where the coupling partners are a boronic acid with a halide catalyzed by a palladium(0) complex. This Thermo

Formula: C₇H₉BO₃

Purity: 97%

Color and Shape: White to pale cream, Crystals or powder or crystalline powder

Molecular weight: 151.96

Ref: 02-B21071

2-Methoxyphenylboronic acid, min. 97%

CAS: 5720-06-9

2-Methoxyphenylboronic acid, min. 97%

Formula: CH₃OC₆H₄B(OH)₂

Purity: min. 97%

Color and Shape: white to off-white pwdr.

Molecular weight: 151.96

Ref: 08-05-0878

2-Methoxyphenylboronic acid

CAS: 5720-06-9

Formula: C₇H₉BO₃

Purity: 98%

Color and Shape: Solid

Molecular weight: 151.9556

Ref: IN-DA003HJR

2-Methoxybenzeneboronic acid

CAS: 5720-06-9

2-Methoxybenzeneboronic acid

Formula: C₇H₉BO₃

Purity: ≥95%

Color and Shape: off-white crystalline solid

Molecular weight: 151.96g/mol

Ref: 54-OR3663

2-Methoxyphenylboronic acid

CAS: 5720-06-9

Formula: C₇H₉BO₃

Purity: ≥ 98.0%

Color and Shape: Off-white powder

Molecular weight: 151.96

Ref: 7W-GK7627

2-Methoxybenzeneboronic acid

CAS: 5720-06-9

Formula: C₇H₉BO₃

Purity: 98%

Color and Shape: Solid, Crystalline Powder or Powder

Molecular weight: 151.96

Ref: 10-F011001

2-Methoxyphenylboronic Acid extrapure, 95%

CAS: 5720-06-9

Formula: C₇H₉BO₃

Purity: min. 95%

Color and Shape: White to off-white, Crystalline powder

Molecular weight: 157.00

Ref: SR-51234

2-Methoxylphenylboronic Acid (contains varying amounts of Anhydride)

Controlled Product

CAS: 5720-06-9

Applications 2-Methoxylphenylboronic Acid is a phenylboronic acid used to investigate boron function in plants.
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),

Formula: C₇H₉BO₃

Color and Shape: Neat

Molecular weight: 151.96

Ref: TR-M260935