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Catalog Number:
40256
CAS Number:
107099-99-0
2,5-Dimethoxyphenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
2,5-Dimethoxybenzeneboronic acid
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Product Information

2,5-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 selective reactions, particularly in Suzuki-Miyaura cross-coupling reactions, which are pivotal in constructing complex organic molecules. Researchers appreciate its role in synthesizing biologically active compounds, including potential anticancer agents and other therapeutic molecules.

Additionally, 2,5-Dimethoxyphenylboronic acid serves as a valuable building block in materials science, particularly in the development of functionalized polymers and organic electronics. Its compatibility with various substrates and ease of modification enhance its applicability in diverse fields, from drug discovery to advanced material fabrication. With its broad range of applications and significant advantages over similar compounds, this boronic acid is a crucial tool for researchers and industry professionals aiming to innovate and optimize their chemical processes.

Synonyms
2,5-Dimethoxybenzeneboronic acid
CAS Number
107099-99-0
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H11BO4
Molecular Weight
181.98
MDL Number
MFCD01318181
PubChem ID
2734342
Melting Point
97 °C (Lit.)
Appearance
White to slightly yellow crystalline powder
Conditions
Store at RT
General Information
Synonyms
2,5-Dimethoxybenzeneboronic acid
CAS Number
107099-99-0
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H11BO4
Molecular Weight
181.98
MDL Number
MFCD01318181
PubChem ID
2734342
Melting Point
97 °C (Lit.)
Appearance
White to slightly yellow 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

2,5-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 in complex organic structures, making it valuable for chemists in drug development.
  • Material Science: The compound is applied in the creation of functional materials, including sensors and polymers, due to its ability to form stable complexes with various substrates.
  • Bioconjugation: It plays a role in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing the development of targeted drug delivery systems.
  • Analytical Chemistry: This boronic acid is utilized in the detection of sugars and other diols, making it useful in various analytical applications, including food safety testing and clinical diagnostics.

Citations