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Catalog Number:
39948
CAS Number:
1385826-84-5
2-([1,1':3',1''-terphényl]-4-yl)-4,4,5,5-tétraméthyl-1,3,2-dioxaborolane
Purity:
≥ 98% (CG)
Synonym(s):
4,4,5,5-tétraméthyl-2-[1,1':3',1''-terphényl]-4-yl-1,3,2-dioxaborolane, Ester pinacol de l'acide (1,1':3',1''-terphényl)-4-ylboronique
Documents
$84.83 /200 mg
Taille
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Product Information

2-([1,1':3',1''-Terphenyl]-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a specialized boron compound known for its unique structural properties and versatility in various applications. This compound features a dioxaborolane ring, which enhances its stability and reactivity, making it an excellent candidate for use in organic synthesis and materials science. Its distinctive terphenyl moiety contributes to its photophysical properties, making it valuable in the development of organic light-emitting diodes (OLEDs) and other optoelectronic devices. Researchers have leveraged this compound in the synthesis of advanced materials, including polymers and nanocomposites, due to its ability to facilitate cross-linking and improve mechanical properties.

In addition to its applications in electronics, this compound is also being explored for its potential in medicinal chemistry, particularly in the design of boron-containing drugs that can target specific biological pathways. Its favorable solubility and compatibility with various solvents make it an attractive option for researchers looking to develop innovative solutions in both industrial and laboratory settings. With its unique features and broad applicability, 2-([1,1':3',1''-Terphenyl]-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane stands out as a valuable resource for professionals in the fields of chemistry, materials science, and pharmaceuticals.

Synonyms
4,4,5,5-tétraméthyl-2-[1,1':3',1''-terphényl]-4-yl-1,3,2-dioxaborolane, Ester pinacol de l'acide (1,1':3',1''-terphényl)-4-ylboronique
CAS Number
1385826-84-5
Purity
≥ 98% (CG)
Molecular Formula
C 24 H 25 BO 2
Molecular Weight
356.27
MDL Number
MFCD32263496
PubChem ID
140763983
Melting Point
99 - 103 ?C
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Conserver à ≤ -4 °C
General Information
Synonyms
4,4,5,5-tétraméthyl-2-[1,1':3',1''-terphényl]-4-yl-1,3,2-dioxaborolane, Ester pinacol de l'acide (1,1':3',1''-terphényl)-4-ylboronique
CAS Number
1385826-84-5
Purity
≥ 98% (CG)
Molecular Formula
C 24 H 25 BO 2
Molecular Weight
356.27
MDL Number
MFCD32263496
PubChem ID
140763983
Melting Point
99 - 103 ?C
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Conserver à ≤ -4 °C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

2-([1,1':3',1''-Terphenyl]-4-yl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in organic synthesis, facilitating the formation of complex molecules through cross-coupling reactions, which are essential in pharmaceuticals and materials science.
  • Fluorescent Materials: It is used in the development of fluorescent materials, particularly in organic light-emitting diodes (OLEDs), enhancing the efficiency and brightness of displays in consumer electronics.
  • Bioconjugation: The chemical plays a significant role in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, which is crucial in drug delivery systems and diagnostic applications.
  • Polymer Chemistry: It is employed in the synthesis of boron-containing polymers, which exhibit unique properties such as thermal stability and electrical conductivity, making them valuable in advanced materials and coatings.
  • Environmental Applications: The compound is explored for its potential in environmental remediation, particularly in the removal of pollutants from water, showcasing its utility in sustainable practices.

Citations