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Catalog Number:
40392
CAS Number:
951677-39-7
2,3-Dichloropyridine-4-boronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
2,3-Dichloro-4-pyridylboronic acid
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Product Information

2,3-Dichloropyridine-4-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 the formation of carbon-carbon bonds. Its unique structure, featuring both a pyridine ring and boronic acid functionality, allows for selective reactivity, making it an excellent choice for the development of complex molecules in pharmaceuticals and agrochemicals. Researchers appreciate its ability to facilitate the synthesis of biologically active compounds, including potential drug candidates and advanced materials.

In addition to its synthetic applications, 2,3-Dichloropyridine-4-boronic acid is also recognized for its potential in the development of sensors and catalysts. Its stability and compatibility with various reaction conditions enhance its appeal in both academic and industrial settings. By incorporating this compound into your research or production processes, you can leverage its unique properties to drive innovation and efficiency in your projects.

Synonyms
2,3-Dichloro-4-pyridylboronic acid
CAS Number
951677-39-7
Purity
97 - 105% (Assay by titration)
Molecular Formula
C5H4BCl2NO2
Molecular Weight
191.8
MDL Number
MFCD04038756
PubChem ID
3478955
Melting Point
141 °C (Lit.)
Appearance
White to almost white crystalline powder
Conditions
Store at RT
General Information
Synonyms
2,3-Dichloro-4-pyridylboronic acid
CAS Number
951677-39-7
Purity
97 - 105% (Assay by titration)
Molecular Formula
C5H4BCl2NO2
Molecular Weight
191.8
MDL Number
MFCD04038756
PubChem ID
3478955
Melting Point
141 °C (Lit.)
Appearance
White to almost 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

2,3-Dichloropyridine-4-boronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of anti-cancer agents, enhancing the efficiency of drug discovery processes.
  • Agricultural Chemistry: It is used in the formulation of herbicides and pesticides, contributing to improved crop protection strategies and sustainable agricultural practices.
  • Material Science: The compound plays a role in the development of advanced materials, such as polymers and composites, which can exhibit enhanced properties like durability and resistance to environmental factors.
  • Organic Synthesis: As a versatile building block, it is employed in various organic reactions, enabling chemists to create complex molecules with specific functionalities, thus streamlining synthetic pathways.
  • Analytical Chemistry: It is utilized in the development of sensors and analytical methods for detecting specific analytes, providing reliable solutions for environmental monitoring and quality control in various industries.

Citations