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Catalog Number:
40120
CAS Number:
3900-89-8
2-Chlorophenylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
2-Chlorobenzeneboronic acid
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Product Information

2-Chlorophenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Researchers and industry professionals appreciate its role in the development of pharmaceuticals, agrochemicals, and advanced materials. Its unique properties enable the formation of carbon-carbon bonds, facilitating the synthesis of complex organic molecules with precision and efficiency.

In addition to its synthetic applications, 2-Chlorophenylboronic acid has shown promise in the field of biochemistry, particularly in the development of targeted drug delivery systems. Its ability to selectively bind to specific biomolecules opens avenues for innovative therapeutic strategies. The compound's stability and reactivity make it a valuable tool for chemists looking to enhance their research and product development efforts. With its broad range of applications, 2-Chlorophenylboronic acid stands out as a key ingredient in the modern chemical landscape.

Synonyms
2-Chlorobenzeneboronic acid
CAS Number
3900-89-8
Purity
95 - 105% (Assay by titration)
Molecular Formula
C6H6BClO2
Molecular Weight
156.37
MDL Number
MFCD00674012
PubChem ID
2734322
Melting Point
92 - 102 °C
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
2-Chlorobenzeneboronic acid
CAS Number
3900-89-8
Purity
95 - 105% (Assay by titration)
Molecular Formula
C6H6BClO2
Molecular Weight
156.37
MDL Number
MFCD00674012
PubChem ID
2734322
Melting Point
92 - 102 °C
Appearance
White to off-white crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Chlorophenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound is crucial in synthesizing various pharmaceuticals, particularly in the development of anti-cancer drugs. Its ability to form stable complexes with biomolecules enhances drug efficacy.
  • Organic Synthesis: It serves as a versatile building block in organic chemistry, facilitating the creation of complex organic molecules through cross-coupling reactions, which are essential in materials science and chemical manufacturing.
  • Bioconjugation: In biochemistry, it is used for labeling biomolecules. Its boronic acid functionality allows for selective binding to diols, making it valuable in creating targeted drug delivery systems.
  • Sensor Technology: This compound is employed in the development of chemical sensors that detect glucose levels, benefiting the medical field, especially in diabetes management, by providing real-time monitoring solutions.
  • Environmental Applications: It is utilized in the remediation of environmental pollutants, particularly in the removal of heavy metals from wastewater, showcasing its role in sustainable practices and environmental protection.

Citations