Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
30879
CAS Number:
5720-06-9
2-Methoxyphenylboronic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
2-Methoxybenzeneboronic acid, o-Anisylboronic acid
Documents
$18.53 /5G
Pack Size Availability Price
Request Bulk Quote
Product Information

2-Methoxyphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Researchers and industry professionals leverage its unique properties to develop pharmaceuticals, agrochemicals, and advanced materials. Its applications extend to the synthesis of biologically active compounds, where it serves as a key building block in the creation of targeted drug candidates.

In addition to its synthetic utility, 2-Methoxyphenylboronic acid exhibits significant potential in the field of sensor technology, particularly in the detection of glucose and other biomolecules. Its selective binding capabilities enhance the sensitivity and specificity of biosensors, making it a valuable tool in medical diagnostics. With its favorable solubility and stability, this compound stands out among similar boronic acids, offering researchers a reliable option for diverse applications in both laboratory and industrial settings.

Synonyms
2-Methoxybenzeneboronic acid, o-Anisylboronic acid
CAS Number
5720-06-9
Purity
≥ 99% (HPLC)
Molecular Formula
C7H9BO3
Molecular Weight
151.96
MDL Number
MFCD00236047
PubChem ID
2733958
Melting Point
105 - 110 ?C
Appearance
White powder
Conditions
Store at RT
General Information
Synonyms
2-Methoxybenzeneboronic acid, o-Anisylboronic acid
CAS Number
5720-06-9
Purity
≥ 99% (HPLC)
Molecular Formula
C7H9BO3
Molecular Weight
151.96
MDL Number
MFCD00236047
PubChem ID
2733958
Melting Point
105 - 110 ?C
Appearance
White powder
Conditions
Store at RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Methoxyphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key reagent in Suzuki-Miyaura cross-coupling reactions, allowing for the formation of carbon-carbon bonds. This is particularly useful in creating complex organic molecules in pharmaceuticals and agrochemicals.
  • Drug Development: It plays a significant role in the synthesis of biologically active compounds, aiding researchers in developing new medications that target various diseases, including cancer.
  • Material Science: The compound is used in the development of advanced materials, such as polymers and nanomaterials, enhancing properties like conductivity and strength.
  • Bioconjugation: It is employed in bioconjugation techniques, which are essential for creating targeted drug delivery systems, improving the efficacy of therapeutic agents.
  • Analytical Chemistry: This chemical is utilized in sensor technology, particularly in the detection of biomolecules, providing a sensitive and selective method for monitoring biological processes.

Citations