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Catalog Number:
40022
CAS Number:
99770-93-1
Éster de bis (pinacol) del ácido 1,4-bencenodiborónico
Purity:
≥ 98% (GC)
Synonym(s):
1,4-Bis(4,4,5,5-Tetrametil-1,3,2-dioxaborolan-2-il)benceno, 1,4-Fenilenobis(4,4,5,5-tetrametil-1,3,2-dioxaborolano)
Documents
$98.65 /5G
Tamaño
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Product Information

1,4-Benzenediboronic acid bis(pinacol) ester is a versatile compound widely utilized in organic synthesis and materials science. This compound serves as a crucial building block in the development of advanced materials, particularly in the synthesis of polymers and organic electronics. Its unique structure allows for effective cross-coupling reactions, making it an essential reagent in the formation of carbon-carbon bonds. Researchers and industry professionals often leverage its properties to create functionalized materials that exhibit enhanced electrical and optical characteristics, which are vital in the production of OLEDs and other electronic devices.

Additionally, 1,4-Benzenediboronic acid bis(pinacol) ester is recognized for its stability and ease of handling, which significantly simplifies laboratory procedures. Its application extends to medicinal chemistry, where it plays a role in the development of pharmaceuticals through its ability to facilitate complex molecular architectures. The compound's compatibility with various reaction conditions further enhances its appeal, making it a preferred choice for chemists seeking reliable and efficient reagents in their synthetic pathways.

Synonyms
1,4-Bis(4,4,5,5-Tetrametil-1,3,2-dioxaborolan-2-il)benceno, 1,4-Fenilenobis(4,4,5,5-tetrametil-1,3,2-dioxaborolano)
CAS Number
99770-93-1
Purity
≥ 98% (GC)
Molecular Formula
C18H28B2O4
Molecular Weight
330.04
MDL Number
MFCD08276852
PubChem ID
10592495
Melting Point
241 - 245 °C
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Tienda en RT
General Information
Synonyms
1,4-Bis(4,4,5,5-Tetrametil-1,3,2-dioxaborolan-2-il)benceno, 1,4-Fenilenobis(4,4,5,5-tetrametil-1,3,2-dioxaborolano)
CAS Number
99770-93-1
Purity
≥ 98% (GC)
Molecular Formula
C18H28B2O4
Molecular Weight
330.04
MDL Number
MFCD08276852
PubChem ID
10592495
Melting Point
241 - 245 °C
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Tienda en RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

1,4-Benzenediboronic acid bis(pinacol) ester is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key reagent in cross-coupling reactions, particularly in the formation of carbon-carbon bonds, which is essential for creating complex organic molecules in pharmaceuticals and materials science.
  • Polymer Chemistry: It is used in the development of advanced polymers, enhancing properties such as strength and thermal stability, making it valuable in industries like automotive and electronics.
  • Bioconjugation: The compound facilitates the attachment of biomolecules in bioconjugation processes, which is crucial for drug delivery systems and diagnostic applications in the biomedical field.
  • Fluorescent Probes: It can be employed in the synthesis of fluorescent probes for imaging applications, aiding researchers in visualizing cellular processes in real-time.
  • Chemical Sensors: This ester is utilized in the fabrication of chemical sensors, providing high sensitivity and selectivity for detecting various analytes, which is beneficial in environmental monitoring and safety applications.

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