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Catalog Number:
40204
CAS Number:
73852-17-2
Acide 2,6-dichlorophénylboronique
Purity:
96 - 105 % (dosage par titrage)
Synonym(s):
Acide 2,6-dichlorobenzèneboronique
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Product Information

2,6-Dichlorophenylboronic 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 properties allow for the selective functionalization of aromatic compounds, facilitating the synthesis of complex molecules. Researchers have successfully employed 2,6-Dichlorophenylboronic acid in Suzuki-Miyaura cross-coupling reactions, which are pivotal in constructing carbon-carbon bonds in the production of advanced materials and biologically active compounds.

Moreover, this compound's application extends to the field of sensor technology, where it is used in the development of chemical sensors for detecting sugars and other biomolecules. Its effectiveness in these applications is enhanced by its high reactivity and selectivity, making it a preferred choice for researchers looking to innovate in synthetic methodologies and analytical techniques. With its broad range of applications and significant advantages over similar compounds, 2,6-Dichlorophenylboronic acid stands out as a crucial tool for professionals in chemistry and related fields.

Synonyms
Acide 2,6-dichlorobenzèneboronique
CAS Number
73852-17-2
Purity
96 - 105 % (dosage par titrage)
Molecular Formula
C6H5BCl2O2
Molecular Weight
190.81
MDL Number
MFCD00064869
PubChem ID
2734332
Melting Point
151 °C (lit.)
Appearance
Poudre cristalline blanche à jaune clair
Conditions
Magasin chez RT
General Information
Synonyms
Acide 2,6-dichlorobenzèneboronique
CAS Number
73852-17-2
Purity
96 - 105 % (dosage par titrage)
Molecular Formula
C6H5BCl2O2
Molecular Weight
190.81
MDL Number
MFCD00064869
PubChem ID
2734332
Melting Point
151 °C (lit.)
Appearance
Poudre cristalline blanche à jaune clair
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

2,6-Dichlorophenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key reagent in Suzuki coupling reactions, enabling the formation of carbon-carbon bonds. This is particularly valuable in the synthesis of pharmaceuticals and agrochemicals.
  • Drug Development: It plays a crucial role in the development of boron-containing drugs, which can enhance the efficacy of treatments for various diseases, including cancer.
  • Material Science: The compound is used in creating advanced materials, such as polymers and nanomaterials, which have applications in electronics and coatings.
  • Bioconjugation: It is employed in bioconjugation techniques to attach biomolecules to surfaces or other molecules, facilitating the development of biosensors and targeted drug delivery systems.
  • Environmental Science: This chemical can be used in the detection and removal of pollutants, contributing to environmental monitoring and remediation efforts.

Citations