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Catalog Number:
40287
CAS Number:
89694-48-4
Ácido 5-cloro-2-metoxifenilborónico
Purity:
95 - 105% (Ensayo por titulación)
Synonym(s):
Ácido 5-cloro-2-metoxibencenoborónico
Documents
$68.20 /5G
Tamaño
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Información del producto

5-Chloro-2-methoxyphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is particularly valued for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Researchers and industry professionals leverage its unique properties to synthesize complex organic molecules, including pharmaceuticals and agrochemicals. Its application in the development of targeted therapies showcases its significance in advancing drug discovery and development.

Additionally, 5-Chloro-2-methoxyphenylboronic acid serves as a key building block in the synthesis of various biologically active compounds. Its compatibility with diverse reaction conditions enhances its utility in laboratory settings, allowing for efficient and selective transformations. With its proven track record in facilitating the formation of carbon-carbon bonds, this compound stands out as a reliable choice for chemists seeking to streamline their synthetic pathways while achieving high yields and purity.

Número CAS
89694-48-4
Fórmula molecular
C7H8BClO3
Peso molecular
186.4
Número MDL
MFCD01318966
Punto de fusión
145 °C (Literatura)
Condiciones
Tienda en RT
Información general
Número CAS
89694-48-4
Fórmula molecular
C7H8BClO3
Peso molecular
186.4
Número MDL
MFCD01318966
Punto de fusión
145 °C (Literatura)
Condiciones
Tienda en RT
Propiedades
¡Pronto habrá más información sobre la propiedad!
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Seguridad y normativas
Materiales peligrosos
-
Antibiótico
-
Regulado por la DEA
No
Advertencias
-
Aplicaciones

5-Chloro-2-methoxyphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key intermediate in the synthesis of various pharmaceuticals and agrochemicals, enabling the development of new drugs and crop protection agents.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds in organic chemistry, making it invaluable for researchers in synthetic chemistry.
  • Bioconjugation: The boronic acid functionality allows for selective binding to diols, making it useful in bioconjugation techniques for labeling biomolecules, enhancing the study of biological processes.
  • Sensor Development: This compound can be employed in the fabrication of chemical sensors for detecting glucose and other biomolecules, which is beneficial in medical diagnostics and monitoring applications.
  • Material Science: It is used in the development of advanced materials, such as polymers and nanomaterials, due to its ability to modify material properties, thus aiding in the creation of innovative products.

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