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Catalog Number:
40227
CAS Number:
23112-96-1
2,6-Dimethoxyphenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
2,6-Dimethoxybenzeneboronic acid
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Product Information

2,6-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 Suzuki-Miyaura cross-coupling, which is crucial for constructing complex organic molecules. Researchers appreciate its role in the synthesis of biologically active compounds, including potential anti-cancer agents and other therapeutic drugs.

Moreover, 2,6-Dimethoxyphenylboronic acid exhibits excellent solubility in organic solvents, enhancing its applicability in diverse chemical reactions. Its low toxicity and favorable handling properties make it a preferred choice for laboratory use. With its strong reactivity and compatibility with various functional groups, this compound stands out as a valuable tool for chemists aiming to innovate in drug discovery and material science. Whether you are developing new pharmaceuticals or exploring advanced materials, 2,6-Dimethoxyphenylboronic acid offers significant advantages in efficiency and effectiveness.

Synonyms
2,6-Dimethoxybenzeneboronic acid
CAS Number
23112-96-1
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H11BO4
Molecular Weight
181.98
MDL Number
MFCD01318987
PubChem ID
2734343
Melting Point
113 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
2,6-Dimethoxybenzeneboronic acid
CAS Number
23112-96-1
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H11BO4
Molecular Weight
181.98
MDL Number
MFCD01318987
PubChem ID
2734343
Melting Point
113 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2,6-Dimethoxyphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key reagent in Suzuki-Miyaura cross-coupling reactions, allowing chemists to create complex organic molecules efficiently. Its ability to form stable boronate esters makes it invaluable in developing pharmaceuticals and agrochemicals.
  • Bioconjugation: It is employed in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules. This application is crucial in the development of targeted drug delivery systems and diagnostic tools.
  • Sensor Development: The compound is used in creating sensors for detecting various analytes, including glucose. Its sensitivity and selectivity make it suitable for applications in medical diagnostics and environmental monitoring.
  • Material Science: In the field of material science, it plays a role in the development of polymeric materials with enhanced properties, such as improved conductivity or mechanical strength, which are essential for electronics and packaging industries.
  • Research in Medicinal Chemistry: It is utilized in the design and synthesis of new drug candidates, particularly in targeting specific biological pathways. Its unique properties allow for modifications that can enhance the efficacy and reduce side effects of therapeutic agents.

Citations