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Catalog Number:
26704
CAS Number:
396102-17-3
Ácido (2,3-dimetoxi-5-metilfenil)borónico
Purity:
≥ 95 % (LCMS)
Documents
$86.23 /25 mg
Tamaño
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Product Information

(2,3-Dimethoxy-5-methylphenyl)boronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued 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 facilitate the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its effectiveness in catalyzing reactions under mild conditions enhances its appeal, allowing for greater efficiency and reduced environmental impact in chemical processes.

In addition to its role in synthetic chemistry, (2,3-Dimethoxy-5-methylphenyl)boronic acid has shown potential in the development of advanced materials and sensors. Its ability to selectively bind to specific biomolecules opens avenues for applications in biochemistry and diagnostics. With its favorable solubility and stability, this compound stands out as a reliable choice for researchers seeking to innovate in various fields, from drug discovery to material science.

CAS Number
396102-17-3
Purity
≥ 95 % (LCMS)
Molecular Formula
C 9 H 13 BO 4
Molecular Weight
196.0
MDL Number
MFCD12827469
PubChem ID
11310092
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
396102-17-3
Purity
≥ 95 % (LCMS)
Molecular Formula
C 9 H 13 BO 4
Molecular Weight
196.0
MDL Number
MFCD12827469
PubChem ID
11310092
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(2,3-Dimethoxy-5-methylphenyl)boronic acid is widely utilized in research focused on

  • Organic Synthesis: This compound serves as a key building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds in complex organic compounds, making it valuable in materials science and drug discovery.
  • Bioconjugation: The unique properties of this boronic acid allow it to selectively bind to diols, facilitating the development of bioconjugates for targeted drug delivery systems in cancer therapy.
  • Sensor Development: Its ability to interact with specific biomolecules makes it useful in creating sensors for detecting glucose levels, which is crucial for diabetes management.
  • Research in Catalysis: This compound is employed in catalytic processes, enhancing reaction efficiency and selectivity, which is beneficial in both academic research and industrial applications.

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