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Catalog Number:
28658
CAS Number:
452972-09-7
Acide 5-bromopyridine-3-boronique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Acide (5-bromo-3-pyridinyl)boronique
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Product Information

5-Bromopyridine-3-boronic acid is a versatile boronic acid derivative that plays a crucial 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 for the synthesis of various biaryl compounds, which are significant in pharmaceuticals and agrochemicals. Its unique bromine substituent enhances its reactivity and selectivity, allowing for the development of complex molecular architectures. Researchers and industry professionals utilize 5-Bromopyridine-3-boronic acid in the design of targeted therapies and in the creation of novel materials, particularly in the fields of drug discovery and material science.

The compound's solubility in common organic solvents and its stability under standard laboratory conditions further enhance its appeal for laboratory applications. Its compatibility with a range of functional groups allows for diverse synthetic pathways, making it a valuable asset in both academic research and industrial applications. With its proven efficacy in facilitating complex reactions, 5-Bromopyridine-3-boronic acid stands out as a key reagent for those looking to innovate in chemical synthesis.

Synonyms
Acide (5-bromo-3-pyridinyl)boronique
CAS Number
452972-09-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C5H5BBrNO2
Molecular Weight
201.81
MDL Number
MFCD02685634
PubChem ID
3814811
Appearance
Poudre blanche à jaune clair
Conditions
Conserver à 0-8 °C
General Information
Synonyms
Acide (5-bromo-3-pyridinyl)boronique
CAS Number
452972-09-7
Purity
≥ 98 % (HPLC)
Molecular Formula
C5H5BBrNO2
Molecular Weight
201.81
MDL Number
MFCD02685634
PubChem ID
3814811
Appearance
Poudre blanche à jaune clair
Conditions
Conserver à 0-8 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

5-Bromopyridine-3-boronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound is crucial in synthesizing various pharmaceuticals, particularly in creating targeted therapies for diseases like cancer. Its boronic acid functionality allows for the formation of stable complexes with biomolecules.
  • Organic Synthesis: It serves as a versatile building block in organic chemistry, facilitating the development of complex organic molecules. Researchers often use it in Suzuki coupling reactions, which are essential for creating carbon-carbon bonds.
  • Agricultural Chemistry: The compound is explored for its potential in developing agrochemicals, including herbicides and pesticides, which can enhance crop protection and yield.
  • Material Science: It is applied in the creation of advanced materials, such as polymers and nanomaterials, where its unique properties can improve material performance and functionality.
  • Diagnostic Tools: The compound is being investigated for use in diagnostic applications, particularly in the development of sensors that can detect specific biomolecules, aiding in early disease detection.

Citations