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Catalog Number:
28466
CAS Number:
151169-75-4
3,4-Dichlorophenylboronic acid
Purity:
≥ 99.5% (HPLC)
Synonym(s):
(3,4-Dichlorophenyl)boranediol
Documents
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Product Information

3,4-Dichlorophenylboronic acid is a versatile organoboron compound recognized for its significant role in organic synthesis and medicinal chemistry. This compound features a boronic acid functional group, which makes it particularly useful in Suzuki-Miyaura cross-coupling reactions, a key method for forming carbon-carbon bonds. Researchers and industry professionals utilize 3,4-Dichlorophenylboronic acid in the development of pharmaceuticals, agrochemicals, and advanced materials, owing to its ability to facilitate the construction of complex molecular architectures. Its unique dichlorophenyl structure enhances its reactivity and selectivity, making it a valuable building block in the synthesis of biologically active compounds.

In addition to its synthetic applications, 3,4-Dichlorophenylboronic acid has shown promise in the field of sensor technology, particularly in the detection of glucose and other biomolecules. The compound's ability to form stable complexes with diols allows for the development of sensitive and selective sensors, which can be crucial for medical diagnostics and environmental monitoring. With its diverse applications and advantages over similar compounds, 3,4-Dichlorophenylboronic acid stands out as an essential tool for researchers and industry professionals seeking innovative solutions in their respective fields.

Synonyms
(3,4-Dichlorophenyl)boranediol
CAS Number
151169-75-4
Purity
≥ 99.5% (HPLC)
Molecular Formula
C6H5BCl2O2
Molecular Weight
190.82
MDL Number
MFCD01074646
PubChem ID
2734330
Appearance
White to off-white crystal
Conditions
Store at 0-8°C
General Information
Synonyms
(3,4-Dichlorophenyl)boranediol
CAS Number
151169-75-4
Purity
≥ 99.5% (HPLC)
Molecular Formula
C6H5BCl2O2
Molecular Weight
190.82
MDL Number
MFCD01074646
PubChem ID
2734330
Appearance
White to off-white crystal
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3,4-Dichlorophenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound is a key intermediate in the synthesis of various pharmaceuticals and agrochemicals, enabling the development of new drugs and crop protection agents.
  • Medicinal Chemistry: It serves as a building block for creating boron-containing compounds, which have shown promise in targeted cancer therapies, enhancing the effectiveness of treatment regimens.
  • Material Science: Used in the development of advanced materials, particularly in creating polymers with unique properties, which can be applied in electronics and coatings.
  • Bioconjugation: It plays a significant role in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, facilitating drug delivery systems.
  • Analytical Chemistry: This compound is utilized in sensor development for detecting various analytes, providing a reliable method for monitoring environmental pollutants and biological markers.

Citations