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Catalog Number:
40246
CAS Number:
40972-86-9
2,3-Dimethoxyphenylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
2,3-Dimethoxybenzeneboronic acid
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Product Information

2,3-Dimethoxyphenylboronic acid is a versatile boronic acid derivative known for its significant role in organic synthesis and medicinal chemistry. This compound features two methoxy groups that enhance its reactivity and solubility, making it an ideal candidate for various applications, including the development of pharmaceuticals and agrochemicals. Its unique structure allows for efficient coupling reactions, particularly in Suzuki-Miyaura cross-coupling, which is pivotal in forming carbon-carbon bonds. Researchers utilize 2,3-Dimethoxyphenylboronic acid to synthesize complex molecules and study biological pathways, owing to its ability to selectively bind to diols and other functional groups.

In addition to its utility in synthetic chemistry, this compound has shown promise in the field of materials science, where it can be employed in the creation of functionalized polymers and advanced materials. Its favorable properties, such as high stability and reactivity, position it as a valuable tool for researchers and industry professionals looking to innovate in drug discovery and material development. With its broad range of applications, 2,3-Dimethoxyphenylboronic acid stands out as a key compound for enhancing research outcomes and driving advancements in various scientific fields.

Synonyms
2,3-Dimethoxybenzeneboronic acid
CAS Number
40972-86-9
Purity
95 - 105% (Assay by titration)
Molecular Formula
C8H11BO4
Molecular Weight
181.98
MDL Number
MFCD02683112
PubChem ID
5156491
Melting Point
68 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
2,3-Dimethoxybenzeneboronic acid
CAS Number
40972-86-9
Purity
95 - 105% (Assay by titration)
Molecular Formula
C8H11BO4
Molecular Weight
181.98
MDL Number
MFCD02683112
PubChem ID
5156491
Melting Point
68 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2,3-Dimethoxyphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Medicinal Chemistry: It is employed in drug discovery processes, especially for creating boron-containing compounds that can enhance the efficacy of certain medications, offering potential advantages over traditional compounds.
  • Material Science: The compound is used in the development of advanced materials, such as polymers and nanomaterials, due to its ability to form stable complexes with various substrates.
  • Bioconjugation: In biological research, it is utilized for labeling biomolecules, enabling scientists to track and study interactions in cellular environments.
  • Catalysis: It acts as a catalyst in various chemical reactions, improving reaction efficiency and selectivity, which is crucial in industrial applications.

Citations