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Catalog Number:
27366
CAS Number:
68716-47-2
Ácido 2,4-diclorofenilborónico
Purity:
≥ 99 % (HPLC)
Synonym(s):
Ácido 2,4-diclorobencenoborónico, (2,4-Diclorofenil)boranodiol
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Product Information

2,4-Dichlorophenylboronic acid is a versatile compound widely recognized for its applications in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valuable in the development of pharmaceuticals, where it serves as a key building block in the synthesis of biologically active molecules. Its unique ability to form reversible covalent bonds with diols makes it an essential reagent in various coupling reactions, including Suzuki-Miyaura cross-coupling, which is pivotal in creating complex organic structures.

In addition to its synthetic utility, 2,4-Dichlorophenylboronic acid has shown promise in the field of materials science, particularly in the development of sensors and polymers. Its properties enable the design of advanced materials with tailored functionalities, enhancing performance in applications such as drug delivery systems and environmental monitoring. Researchers and industry professionals can leverage this compound's unique characteristics to innovate and improve existing processes, making it a valuable addition to any laboratory or production facility.

Synonyms
Ácido 2,4-diclorobencenoborónico, (2,4-Diclorofenil)boranodiol
CAS Number
68716-47-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C6H5BCl2O2
Molecular Weight
190.82
MDL Number
MFCD00013930
PubChem ID
2734659
Melting Point
246-249 ?C
Appearance
Polvo cristalino de color blanco a ligeramente amarillo.
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Ácido 2,4-diclorobencenoborónico, (2,4-Diclorofenil)boranodiol
CAS Number
68716-47-2
Purity
≥ 99 % (HPLC)
Molecular Formula
C6H5BCl2O2
Molecular Weight
190.82
MDL Number
MFCD00013930
PubChem ID
2734659
Melting Point
246-249 ?C
Appearance
Polvo cristalino de color blanco a ligeramente amarillo.
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2,4-Dichlorophenylboronic acid is widely utilized in research focused on:

  • Synthesis of Pharmaceuticals: This compound is crucial in the development of various drugs, particularly in creating boronic acid derivatives that are effective in treating cancer and diabetes.
  • Organic Synthesis: It serves as a key reagent in Suzuki coupling reactions, enabling the formation of carbon-carbon bonds, which is essential in the synthesis of complex organic molecules.
  • Bioconjugation: The compound is used in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing the development of targeted therapies and diagnostics.
  • Sensor Development: It plays a role in the creation of chemical sensors for detecting glucose and other analytes, benefiting the medical field by improving diabetes management.
  • Material Science: This chemical is applied in the development of advanced materials, such as polymers and nanomaterials, which have applications in electronics and environmental remediation.

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