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Catalog Number:
40200
CAS Number:
183158-34-1
2,3-Dimethylphenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
2,3-Dimethylbenzeneboronic acid, o-Xylene-3-boronic acid
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Product Information

2,3-Dimethylphenylboronic 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 the development of various pharmaceuticals and agrochemicals. Its unique structure allows for selective reactions, which can enhance the efficiency of synthetic pathways in the production of complex organic molecules. Researchers often employ 2,3-Dimethylphenylboronic acid in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds that are crucial in the synthesis of biologically active compounds.

Moreover, this compound's properties make it an excellent candidate for applications in sensor technology and materials science. Its ability to interact with specific biomolecules opens avenues for the development of innovative diagnostic tools. With its favorable reactivity and functional versatility, 2,3-Dimethylphenylboronic acid stands out as a valuable asset for researchers and industry professionals seeking to advance their projects in organic synthesis and beyond.

Synonyms
2,3-Dimethylbenzeneboronic acid, o-Xylene-3-boronic acid
CAS Number
183158-34-1
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H11BO2
Molecular Weight
149.98
MDL Number
MFCD01863524
PubChem ID
2773395
Melting Point
175 °C (Lit.)
Appearance
White to light yellow crystalline powder
Conditions
Store at RT
General Information
Synonyms
2,3-Dimethylbenzeneboronic acid, o-Xylene-3-boronic acid
CAS Number
183158-34-1
Purity
97 - 105% (Assay by titration)
Molecular Formula
C8H11BO2
Molecular Weight
149.98
MDL Number
MFCD01863524
PubChem ID
2773395
Melting Point
175 °C (Lit.)
Appearance
White to light 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

2,3-Dimethylphenylboronic 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, enhancing the efficiency of chemical reactions.
  • Drug Development: It plays a crucial role in medicinal chemistry, where it is used to create boron-containing compounds that can improve the efficacy of drug candidates, particularly in targeting specific biological pathways.
  • Materials Science: The compound is employed in the production of advanced materials, including polymers and nanomaterials, which can exhibit unique properties beneficial for electronics and coatings.
  • Bioconjugation: It is utilized in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is essential in the development of biosensors and targeted drug delivery systems.
  • Environmental Applications: This chemical is also explored in environmental chemistry for the detection and removal of pollutants, contributing to cleaner technologies and sustainable practices.

Citations