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Catalog Number:
28736
CAS Number:
351019-18-6
Ácido 2-fluoropiridina-5-borónico
Purity:
≥ 98 % (HPLC)
Synonym(s):
Ácido 6-fluoro-3-piridinilborónico
Documents
$18.53 /1G
Tamaño
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Información del producto

2-Fluoropyridine-5-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 invaluable for the formation of carbon-carbon bonds. Its unique fluorine substitution enhances its reactivity and selectivity, allowing researchers to develop complex molecular architectures with precision. This property is particularly beneficial in the pharmaceutical industry, where it is used to synthesize various biologically active compounds, including potential drug candidates.

In addition to its synthetic applications, 2-Fluoropyridine-5-boronic acid is also utilized in the development of agrochemicals and materials science, where its boronic acid functionality can be employed in sensor technology and polymer chemistry. Its compatibility with various reaction conditions and its ability to form stable complexes with diols make it a preferred choice for researchers looking to innovate in these fields. With its broad range of applications and unique properties, this compound is an essential tool for professionals seeking to advance their projects in organic synthesis and beyond.

Número CAS
351019-18-6
Fórmula molecular
C5H5BFNO2
Peso molecular
140.91
Número MDL
MFCD03411559
Condiciones
Conservar entre 0 y 8 °C.
Información general
Número CAS
351019-18-6
Fórmula molecular
C5H5BFNO2
Peso molecular
140.91
Número MDL
MFCD03411559
Condiciones
Conservar entre 0 y 8 °C.
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
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Aplicaciones

2-Fluoropyridine-5-boronic acid is widely utilized in research focused on:

  • Synthetic Chemistry: This compound serves as a key building block in the synthesis of various pharmaceuticals and agrochemicals, enabling the development of new drugs with enhanced efficacy.
  • Drug Discovery: It is employed in medicinal chemistry for the design of novel compounds, particularly in targeting specific biological pathways, which can lead to breakthroughs in treatment options.
  • Material Science: The compound is used in the development of advanced materials, including polymers and coatings, which can exhibit improved properties such as durability and resistance to environmental factors.
  • Bioconjugation: It plays a significant role in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, facilitating studies in biochemistry and molecular biology.
  • Analytical Chemistry: This boronic acid derivative is utilized in various analytical methods, including chromatography and spectroscopy, to enhance the detection and quantification of specific analytes in complex mixtures.

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