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Catalog Number:
39928
CAS Number:
475250-52-3
2-(4-Metoxibencil)-4,4,5,5-tetrametil-1,3,2-dioxaborolano
Purity:
≥ 97% (GC)
Synonym(s):
Éster de pinacol del ácido 4-metoxibencilborónico
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$436.05 /5G
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Product Information

2-(4-Methoxybenzyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane is a versatile boron-containing compound known for its unique properties that make it valuable in various applications, particularly in organic synthesis and medicinal chemistry. This compound serves as an effective reagent in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds, which is essential in the development of pharmaceuticals and agrochemicals. Its stability and ease of handling further enhance its appeal for researchers looking to streamline their synthetic processes.

Additionally, the compound's methoxy group contributes to its solubility and reactivity, making it suitable for use in diverse chemical environments. Researchers have utilized this compound in the synthesis of complex organic molecules, showcasing its potential in drug discovery and material science. The unique structure of 2-(4-Methoxybenzyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane allows for selective functionalization, providing an edge over similar compounds in terms of efficiency and yield in synthetic applications.

Synonyms
Éster de pinacol del ácido 4-metoxibencilborónico
CAS Number
475250-52-3
Purity
≥ 97% (GC)
Molecular Formula
C 14 H 21 BO 3
Molecular Weight
248.13
MDL Number
MFCD10698526
PubChem ID
12012759
Density
1,02 g/ml
Appearance
Líquido transparente e incoloro
Refractive Index
n20D 1,50
Conditions
Conservar entre 2 y 8 °C.
General Information
Synonyms
Éster de pinacol del ácido 4-metoxibencilborónico
CAS Number
475250-52-3
Purity
≥ 97% (GC)
Molecular Formula
C 14 H 21 BO 3
Molecular Weight
248.13
MDL Number
MFCD10698526
PubChem ID
12012759
Density
1,02 g/ml
Appearance
Líquido transparente e incoloro
Refractive Index
n20D 1,50
Conditions
Conservar entre 2 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-(4-Methoxybenzyl)-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 chemistry, facilitating the formation of carbon-carbon bonds, which is essential for synthesizing complex molecules.
  • Medicinal Chemistry: It plays a crucial role in drug development, particularly in the design of pharmaceuticals that target specific biological pathways, enhancing efficacy and reducing side effects.
  • Materials Science: The compound is used in the development of advanced materials, including polymers and coatings, due to its unique chemical properties that improve durability and performance.
  • Bioconjugation: It is employed in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is vital for diagnostics and therapeutic applications.
  • Analytical Chemistry: This chemical is utilized in various analytical methods, such as chromatography and spectroscopy, aiding in the detection and quantification of other compounds in complex mixtures.

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