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Catalog Number:
28088
CAS Number:
6165-69-1
Acide thiophène-3-boronique
Purity:
≥ 98 % (HPLC)
Synonym(s):
Acide 3-thiénylboronique
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Product Information

Thiophene-3-boronic acid is a versatile organoboron compound known for its unique properties and applications in organic synthesis and materials science. This compound features a thiophene ring, which enhances its electronic properties, making it an excellent candidate for use in the development of organic semiconductors and photovoltaic devices. Its boronic acid functionality allows for easy coupling reactions, particularly in Suzuki-Miyaura cross-coupling reactions, which are pivotal in the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Researchers appreciate its ability to form stable complexes with various substrates, facilitating the development of novel materials with tailored properties.

In addition to its role in organic synthesis, Thiophene-3-boronic acid is also utilized in the production of advanced materials such as conductive polymers and sensors. Its unique structure contributes to improved conductivity and stability in these applications, making it a valuable component in the development of next-generation electronic devices. With its combination of reactivity and stability, Thiophene-3-boronic acid stands out as a key ingredient for researchers and industry professionals looking to innovate in the fields of organic chemistry and materials science.

Synonyms
Acide 3-thiénylboronique
CAS Number
6165-69-1
Purity
≥ 98 % (HPLC)
Molecular Formula
C 4 H 5 B O 2 S
Molecular Weight
127.96
MDL Number
MFCD00151851
PubChem ID
581760
Appearance
Poudre blanche à blanc cassé
Conditions
Conserver à 0 - 8 °C
General Information
Synonyms
Acide 3-thiénylboronique
CAS Number
6165-69-1
Purity
≥ 98 % (HPLC)
Molecular Formula
C 4 H 5 B O 2 S
Molecular Weight
127.96
MDL Number
MFCD00151851
PubChem ID
581760
Appearance
Poudre blanche à blanc cassé
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

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

  • Organic Synthesis: This compound serves as a key building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals. Its unique structure allows for the formation of complex compounds through cross-coupling reactions.
  • Material Science: In the field of material science, it is used to create conductive polymers and organic electronic materials. These materials are essential for the development of flexible electronics and solar cells, offering advantages over traditional materials.
  • Bioconjugation: Thiophene-3-boronic acid is employed in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules. This application is crucial in the development of biosensors and targeted drug delivery systems.
  • Catalysis: It acts as a catalyst in various chemical reactions, enhancing reaction rates and selectivity. This property is particularly beneficial in industrial processes, leading to more efficient production methods and reduced waste.
  • Research in Medicinal Chemistry: The compound is actively researched for its potential therapeutic applications. Its ability to interact with biological systems makes it a candidate for drug development, particularly in targeting specific diseases.

Citations