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Catalog Number:
40209
CAS Number:
133730-34-4
2,4-Dimethoxyphenylboronic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
2,4-Dimethoxybenzeneboronic acid
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Product Information

2,4-Dimethoxyphenylboronic 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 the development of various pharmaceuticals and agrochemicals. Its unique structure allows for efficient coupling reactions, particularly in the synthesis of complex organic molecules through Suzuki-Miyaura cross-coupling reactions. Researchers appreciate its role in the preparation of biologically active compounds, including potential anticancer agents and other therapeutic molecules.

In addition to its applications in drug discovery, 2,4-Dimethoxyphenylboronic acid is also employed in materials science for the development of functional materials and sensors. Its ability to selectively bind to specific substrates enhances its utility in creating advanced materials with tailored properties. The compound's stability and reactivity make it a preferred choice for researchers looking to streamline their synthetic pathways while achieving high yields. With its broad range of applications, 2,4-Dimethoxyphenylboronic acid stands out as a valuable tool for both academic and industrial chemists.

Synonyms
2,4-Dimethoxybenzeneboronic acid
CAS Number
133730-34-4
Purity
≥ 99% (HPLC)
Molecular Formula
C8H11BO4
Molecular Weight
181.98
MDL Number
MFCD01074590
PubChem ID
2734341
Melting Point
127 - 130 °C
Appearance
Off-white powder
Conditions
Store at RT
General Information
Synonyms
2,4-Dimethoxybenzeneboronic acid
CAS Number
133730-34-4
Purity
≥ 99% (HPLC)
Molecular Formula
C8H11BO4
Molecular Weight
181.98
MDL Number
MFCD01074590
PubChem ID
2734341
Melting Point
127 - 130 °C
Appearance
Off-white 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

2,4-Dimethoxyphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile 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, making it valuable in the production of complex organic compounds.
  • Bioconjugation: The boronic acid functionality enables selective binding to diols, facilitating the development of bioconjugates for drug delivery systems and diagnostic applications.
  • Material Science: This compound is applied in the creation of advanced materials, such as polymers and nanocomposites, enhancing their properties through boron chemistry.
  • Sensor Development: Its ability to interact with sugars and other biomolecules makes it useful in designing sensors for glucose monitoring and other biochemical applications.

Citations