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Catalog Number:
40361
CAS Number:
108847-76-3
Ácido 1-tiantrenilborónico
Purity:
95 - 105% (Ensayo por titulación)
Synonym(s):
Ácido tiantreno-1-borónico
Documents
$29.34 /1G
Tamaño
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Información del producto

1-Thianthrenylboronic acid is a versatile compound recognized for its unique boronic acid functionality, which makes it an essential building block in organic synthesis and medicinal chemistry. This compound features a thianthrene moiety that enhances its reactivity and selectivity in various chemical reactions. Its ability to form stable complexes with diols and other nucleophiles allows for applications in the development of sensors, drug delivery systems, and as a key intermediate in the synthesis of biologically active molecules. Researchers appreciate its role in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the formation of carbon-carbon bonds, facilitating the creation of complex organic structures.

In addition to its synthetic utility, 1-Thianthrenylboronic acid is gaining attention in the field of materials science, particularly in the development of organic semiconductors and photovoltaic devices. Its unique electronic properties and structural characteristics make it a candidate for innovative applications in optoelectronics. With its diverse applications and significant advantages over similar compounds, 1-Thianthrenylboronic acid stands out as a valuable resource for researchers and industry professionals aiming to push the boundaries of chemical synthesis and material development.

Número CAS
108847-76-3
Fórmula molecular
C12H9BO2S2
Peso molecular
260.13
Número MDL
MFCD00093039
Punto de fusión
148 °C (Literatura)
Condiciones
Tienda en RT
Información general
Número CAS
108847-76-3
Fórmula molecular
C12H9BO2S2
Peso molecular
260.13
Número MDL
MFCD00093039
Punto de fusión
148 °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
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Aplicaciones

1-Thianthrenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Bioconjugation: It is employed in bioconjugation reactions, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing drug delivery systems and diagnostic tools.
  • Material Science: The compound is used to create novel materials with unique electronic properties, making it valuable in the development of organic semiconductors and sensors.
  • Catalysis: 1-Thianthrenylboronic acid acts as a catalyst in various chemical reactions, improving reaction efficiency and selectivity, which is crucial in industrial applications.
  • Research in Medicinal Chemistry: It plays a significant role in the design of new therapeutic agents, particularly in targeting specific biological pathways, offering potential advantages over traditional compounds.

Citas