Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
31439
CAS Number:
871126-15-7
3-Fluoro-2-formylphenylboronic acid
Purity:
≥ 99.5% (HPLC)
Synonym(s):
3-Fluoro-2-formylbenzeneboronic acid
Hazmat
Documents
$29.34 /5G
Pack Size Availability Price
Request Bulk Quote
Product Information

3-Fluoro-2-formylphenylboronic acid is a versatile compound that plays a significant role in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it a valuable building block for the synthesis of complex organic molecules. Its unique fluorine substituent enhances its reactivity and selectivity, which is particularly beneficial in the development of pharmaceuticals and agrochemicals. Researchers appreciate its utility in creating diverse compounds, including biologically active molecules and functional materials.

The compound's boronic acid functionality allows for the formation of stable complexes with diols, which is advantageous in various applications, including sensor technology and drug delivery systems. Its potential to act as a key intermediate in the synthesis of novel therapeutic agents makes it an essential choice for researchers focused on drug discovery and development. With its favorable properties and broad applicability, 3-Fluoro-2-formylphenylboronic acid stands out as a critical reagent in advancing chemical research and innovation.

Synonyms
3-Fluoro-2-formylbenzeneboronic acid
CAS Number
871126-15-7
Purity
≥ 99.5% (HPLC)
Molecular Formula
C7H6BFO3
Molecular Weight
167.93
MDL Number
MFCD10697421
PubChem ID
53412038
Melting Point
123 - 127 ?C
Appearance
White to off-white powder
Conditions
Store at 2-8 °C
General Information
Synonyms
3-Fluoro-2-formylbenzeneboronic acid
CAS Number
871126-15-7
Purity
≥ 99.5% (HPLC)
Molecular Formula
C7H6BFO3
Molecular Weight
167.93
MDL Number
MFCD10697421
PubChem ID
53412038
Melting Point
123 - 127 ?C
Appearance
White to off-white powder
Conditions
Store at 2-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
Yes
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-Fluoro-2-formylphenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as an essential building block in the synthesis of various pharmaceuticals, particularly in creating targeted therapies for diseases such as cancer.
  • Organic Synthesis: It plays a crucial role in cross-coupling reactions, allowing chemists to create complex organic molecules efficiently, which is vital in developing new materials and chemicals.
  • Bioconjugation: The unique properties of this boronic acid facilitate the attachment of biomolecules, enhancing drug delivery systems and improving the efficacy of therapeutic agents.
  • Sensor Technology: Its ability to interact with specific biomolecules makes it useful in designing sensors for detecting glucose levels, which is beneficial for diabetes management.
  • Material Science: The compound is utilized in the development of advanced materials, such as polymers, that exhibit enhanced properties for applications in electronics and coatings.

Citations