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Catalog Number:
28688
CAS Number:
148493-34-9
2,6-Dichloropyridine-3-boronic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
2,6-Dichloro-3-pyridyl boronic acid
Documents
$43.87 /1G
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Product Information

2,6-Dichloropyridine-3-boronic acid is a versatile compound widely utilized in the field of 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 effective coordination with various substrates, making it an ideal candidate for the development of complex organic molecules. Researchers have successfully employed this compound in the synthesis of pharmaceuticals, agrochemicals, and advanced materials, showcasing its relevance across multiple industries.

In addition to its synthetic applications, 2,6-Dichloropyridine-3-boronic acid exhibits potential in the development of targeted therapies due to its ability to interact with biological systems. Its stability and reactivity make it a valuable tool for chemists looking to innovate in drug design and development. With its proven track record in enhancing reaction efficiency and product yield, this compound stands out as a reliable choice for professionals seeking to push the boundaries of chemical research and application.

Synonyms
2,6-Dichloro-3-pyridyl boronic acid
CAS Number
148493-34-9
Purity
≥ 99% (HPLC)
Molecular Formula
C5H4BCl2NO2
Molecular Weight
191.81
MDL Number
MFCD03094989
PubChem ID
2762712
Appearance
Off-white to light yellow powder
Conditions
Store at 0-8°C
General Information
Synonyms
2,6-Dichloro-3-pyridyl boronic acid
CAS Number
148493-34-9
Purity
≥ 99% (HPLC)
Molecular Formula
C5H4BCl2NO2
Molecular Weight
191.81
MDL Number
MFCD03094989
PubChem ID
2762712
Appearance
Off-white to light yellow 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

2,6-Dichloropyridine-3-boronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a crucial building block in the synthesis of various pharmaceuticals, particularly in the development of anti-cancer agents and other therapeutic drugs.
  • Agricultural Chemistry: It is used in the formulation of agrochemicals, including herbicides and pesticides, providing effective solutions for crop protection and yield enhancement.
  • Material Science: The compound plays a role in the creation of advanced materials, such as polymers and coatings, which require specific chemical properties for enhanced durability and performance.
  • Organic Synthesis: It is a valuable reagent in organic chemistry for cross-coupling reactions, allowing chemists to create complex molecules efficiently and with high specificity.
  • Bioconjugation: This chemical is employed in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in diagnostics and therapeutic applications.

Citations