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Catalog Number:
40334
CAS Number:
170981-41-6
2,3-Difluoro-4-methoxyphenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
2,3-Difluoro-4-methoxybenzeneboronic acid
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Product Information

2,3-Difluoro-4-methoxyphenylboronic acid is a versatile boronic acid derivative that has garnered attention in various fields, particularly in medicinal chemistry and organic synthesis. This compound is characterized by its unique difluoro and methoxy substituents, which enhance its reactivity and selectivity in cross-coupling reactions, making it an invaluable tool for researchers aiming to develop complex organic molecules. Its ability to form stable complexes with diols and other Lewis bases allows for applications in the synthesis of pharmaceuticals, agrochemicals, and advanced materials.

In addition to its synthetic utility, 2,3-Difluoro-4-methoxyphenylboronic acid is also being explored for its potential in targeted drug delivery systems and as a building block in the development of novel therapeutic agents. The compound's favorable properties, such as its solubility and stability, further support its use in various research applications. Researchers and industry professionals can leverage this compound to streamline their synthesis processes and enhance the efficacy of their products.

Synonyms
2,3-Difluoro-4-methoxybenzeneboronic acid
CAS Number
170981-41-6
Purity
97 - 105% (Assay by titration)
Molecular Formula
C7H7BF2O3
Molecular Weight
187.94
MDL Number
MFCD07368234
PubChem ID
25067272
Appearance
White to light orange to green powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
2,3-Difluoro-4-methoxybenzeneboronic acid
CAS Number
170981-41-6
Purity
97 - 105% (Assay by titration)
Molecular Formula
C7H7BF2O3
Molecular Weight
187.94
MDL Number
MFCD07368234
PubChem ID
25067272
Appearance
White to light orange to green 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

2,3-Difluoro-4-methoxyphenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound plays a crucial role in the synthesis of various pharmaceuticals, particularly in the development of targeted therapies for cancer treatment, enhancing drug efficacy and specificity.
  • Organic Synthesis: It serves as a versatile building block in organic chemistry, facilitating the creation of complex molecules through cross-coupling reactions, which are essential in the production of agrochemicals and fine chemicals.
  • Material Science: Used in the formulation of advanced materials, it contributes to the development of polymers and coatings with improved properties, such as enhanced durability and chemical resistance.
  • Bioconjugation: This compound is valuable in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is vital for diagnostics and therapeutic applications.
  • Fluorescent Probes: It can be utilized in the design of fluorescent probes for biological imaging, aiding researchers in visualizing cellular processes and understanding disease mechanisms.

Citations