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Catalog Number:
40359
CAS Number:
847664-64-6
2,5-Dichloropyridine-4-boronic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
2,5-Dichloro-4-pyridylboronic acid
Documents
$129.19 /1G
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Product Information

2,5-Dichloropyridine-4-boronic acid is a versatile boronic acid derivative that plays a significant role in organic synthesis and medicinal chemistry. This compound is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block in the development of pharmaceuticals and agrochemicals. Its unique structure, featuring both a pyridine ring and boronic acid functionality, allows for the formation of carbon-carbon bonds, which is crucial in the synthesis of complex organic molecules. Researchers and industry professionals utilize this compound to create a variety of biologically active compounds, including potential drug candidates and advanced materials.

With its high reactivity and selectivity, 2,5-Dichloropyridine-4-boronic acid stands out among similar compounds, offering enhanced efficiency in synthetic pathways. Its applications extend to the development of fluorescent probes and sensors, as well as in the field of catalysis. The compound's stability and ease of handling further contribute to its appeal in laboratory settings, making it a valuable addition to any chemist's toolkit. Whether you are involved in drug discovery or materials science, this compound provides the versatility and performance needed to advance your projects.

Synonyms
2,5-Dichloro-4-pyridylboronic acid
CAS Number
847664-64-6
Purity
≥ 98% (HPLC)
Molecular Formula
C5H4BCl2NO2
Molecular Weight
191.8
MDL Number
MFCD06798254
PubChem ID
12177416
Melting Point
202 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
General Information
Synonyms
2,5-Dichloro-4-pyridylboronic acid
CAS Number
847664-64-6
Purity
≥ 98% (HPLC)
Molecular Formula
C5H4BCl2NO2
Molecular Weight
191.8
MDL Number
MFCD06798254
PubChem ID
12177416
Melting Point
202 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at 2 - 8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2,5-Dichloropyridine-4-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 creating compounds that target specific biological pathways.
  • Agricultural Chemistry: It is used in the formulation of agrochemicals, providing effective solutions for pest control and enhancing crop yields through targeted action.
  • Material Science: The compound plays a role in developing advanced materials, such as polymers and coatings, that require specific chemical properties for improved performance.
  • Organic Synthesis: It is a valuable reagent in organic synthesis, facilitating the formation of carbon-boron bonds, which are essential in creating complex organic molecules.
  • Analytical Chemistry: This chemical is utilized in various analytical techniques, aiding in the detection and quantification of other compounds in complex mixtures.

Citations