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Catalog Number:
28689
CAS Number:
381248-04-0
2-Chloropyridine-3-boronic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
2-Chloro-3-pyridineboronic acid
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$22.03 /1G
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Product Information

2-Chloropyridine-3-boronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its role in Suzuki-Miyaura cross-coupling reactions, which are essential for forming carbon-carbon bonds in the development of pharmaceuticals and agrochemicals. Its unique structure, featuring a chlorine atom and a boronic acid functional group, enhances its reactivity and selectivity, making it an ideal building block for complex molecular architectures. Researchers and industry professionals appreciate its application in the synthesis of biologically active compounds, including potential drug candidates and advanced materials.

In addition to its synthetic utility, 2-Chloropyridine-3-boronic acid exhibits notable advantages over similar compounds, such as improved solubility and stability under various reaction conditions. This makes it a preferred choice for chemists looking to streamline their processes while achieving high yields. Its relevance extends to the fields of agrochemistry and materials science, where it can be employed in the development of novel pesticides and functional materials. With its broad applicability and efficiency, 2-Chloropyridine-3-boronic acid is an essential tool for advancing research and innovation.

Synonyms
2-Chloro-3-pyridineboronic acid
CAS Number
381248-04-0
Purity
≥ 98% (HPLC)
Molecular Formula
C5H5BClNO2
Molecular Weight
157.36
MDL Number
MFCD03094997
PubChem ID
2762704
Melting Point
128-130 °C
Appearance
White or off-white crystalline powder
Conditions
Store at 0-8°C
General Information
Synonyms
2-Chloro-3-pyridineboronic acid
CAS Number
381248-04-0
Purity
≥ 98% (HPLC)
Molecular Formula
C5H5BClNO2
Molecular Weight
157.36
MDL Number
MFCD03094997
PubChem ID
2762704
Melting Point
128-130 °C
Appearance
White or off-white crystalline powder
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

2-Chloropyridine-3-boronic acid is widely utilized in research focused on:

  • Synthetic Chemistry: This compound serves as a versatile building block in the synthesis of various pharmaceuticals and agrochemicals, enabling the development of new drugs and crop protection agents.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds in organic synthesis, thus streamlining the production of complex molecules.
  • Bioconjugation: The boronic acid functionality allows for selective binding to diols, making it useful in bioconjugation applications, such as attaching drugs to targeting molecules for improved therapeutic efficacy.
  • Material Science: In the development of advanced materials, this compound can be utilized in the synthesis of polymers and nanomaterials, enhancing properties like conductivity and mechanical strength.
  • Diagnostics: Its ability to interact with specific biomolecules positions it as a candidate for use in diagnostic applications, particularly in the detection of certain diseases through biomarker identification.

Citations