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Catalog Number:
40361
CAS Number:
108847-76-3
Acide 1-thianthrénylboronique
Purity:
95 - 105 % (dosage par titrage)
Synonym(s):
Acide thianthrène-1-boronique
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Product Information

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.

Synonyms
Acide thianthrène-1-boronique
CAS Number
108847-76-3
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 12 H 9 B O 2 S 2
Molecular Weight
260.13
MDL Number
MFCD00093039
PubChem ID
2734382
Melting Point
148 °C (lit.)
Appearance
Poudre blanche à orange clair à verte
Conditions
Magasin chez RT
General Information
Synonyms
Acide thianthrène-1-boronique
CAS Number
108847-76-3
Purity
95 - 105 % (dosage par titrage)
Molecular Formula
C 12 H 9 B O 2 S 2
Molecular Weight
260.13
MDL Number
MFCD00093039
PubChem ID
2734382
Melting Point
148 °C (lit.)
Appearance
Poudre blanche à orange clair à verte
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

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.

Citations