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Catalog Number:
39908
CAS Number:
269409-97-4
2-(4,4,5,5-Tetrametil-1,3,2-dioxaborolan-2-il)fenol
Purity:
≥ 97,5 % (HPLC)
Synonym(s):
2-(2-hidroxifenil)-4,4,5,5-tetrametil-1,3,2-dioxaborolano, Éster de pinacol del ácido 2-hidroxifenilborónico
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Product Information

2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol is a versatile compound widely recognized for its applications in organic synthesis and materials science. This compound, often referred to as a boron-containing phenol, exhibits unique properties that make it particularly valuable in the development of advanced materials and pharmaceuticals. Its structure allows for effective participation in cross-coupling reactions, which are essential in the synthesis of complex organic molecules. Researchers and industry professionals utilize this compound in the creation of functionalized polymers, agrochemicals, and as a key intermediate in the production of various bioactive compounds.

The stability and reactivity of 2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol make it an excellent choice for applications in medicinal chemistry and materials development. Its ability to form stable complexes with various substrates enhances its utility in catalysis and organic transformations. Additionally, the compound's favorable solubility characteristics facilitate its use in diverse solvent systems, making it adaptable for various laboratory and industrial processes. With its broad range of applications and unique properties, this compound stands out as a valuable asset for researchers and manufacturers alike.

Synonyms
2-(2-hidroxifenil)-4,4,5,5-tetrametil-1,3,2-dioxaborolano, Éster de pinacol del ácido 2-hidroxifenilborónico
CAS Number
269409-97-4
Purity
≥ 97,5 % (HPLC)
Molecular Formula
C 12 H 17 BO 3
Molecular Weight
220.08
MDL Number
MFCD02093754
PubChem ID
2734622
Density
1,06 g/ml
Appearance
Líquido transparente incoloro a ligeramente amarillo.
Boiling Point
94 °C / 0,2 mmHg (Literatura)
Refractive Index
n20D 1,51
Conditions
Tienda en RT
General Information
Synonyms
2-(2-hidroxifenil)-4,4,5,5-tetrametil-1,3,2-dioxaborolano, Éster de pinacol del ácido 2-hidroxifenilborónico
CAS Number
269409-97-4
Purity
≥ 97,5 % (HPLC)
Molecular Formula
C 12 H 17 BO 3
Molecular Weight
220.08
MDL Number
MFCD02093754
PubChem ID
2734622
Density
1,06 g/ml
Appearance
Líquido transparente incoloro a ligeramente amarillo.
Boiling Point
94 °C / 0,2 mmHg (Literatura)
Refractive Index
n20D 1,51
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

2-(4,4,5,5-Tetramethyl-1,3,2-dioxaborolan-2-yl)phenol is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile reagent in organic chemistry, particularly in the synthesis of complex molecules. Its unique structure allows for efficient coupling reactions, making it valuable for researchers developing new pharmaceuticals.
  • Material Science: It is used in the development of advanced materials, including polymers and coatings. The compound enhances the properties of materials, such as thermal stability and mechanical strength, which is crucial in industries like automotive and aerospace.
  • Bioconjugation: This chemical plays a significant role in bioconjugation processes, where it is used to attach biomolecules to surfaces or other molecules. This application is essential in the fields of biotechnology and diagnostics, improving the efficacy of drug delivery systems.
  • Fluorescent Probes: It is utilized in the creation of fluorescent probes for biological imaging. The compound's properties allow for high sensitivity and specificity, aiding researchers in studying cellular processes and disease mechanisms.
  • Environmental Monitoring: The compound is also applied in environmental science for detecting pollutants. Its ability to form stable complexes with certain contaminants makes it a useful tool for monitoring water quality and ensuring environmental safety.

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