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Catalog Number:
40131
CAS Number:
213211-69-9
Ácido 2-etoxifenilborónico
Purity:
≥ 95% (Ensayo por titulación)
Synonym(s):
Ácido 2-etoxibencenoborónico
Documents
$33.75 /1G
Tamaño
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Product Information

2-Ethoxyphenylboronic acid is a versatile organoboron compound recognized for its significant role in organic synthesis and medicinal chemistry. This compound features a boronic acid functional group, which allows it to participate in various coupling reactions, particularly in the formation of carbon-carbon bonds. Its unique structure enhances its reactivity and selectivity, making it an ideal candidate for applications in the development of pharmaceuticals and agrochemicals. Researchers have utilized 2-Ethoxyphenylboronic acid in Suzuki-Miyaura cross-coupling reactions, facilitating the synthesis of complex organic molecules with precision and efficiency.

Moreover, this compound exhibits excellent solubility in organic solvents, which further broadens its applicability in laboratory settings. Its ability to form stable complexes with diols makes it valuable in sensor technology and materials science. As a result, 2-Ethoxyphenylboronic acid stands out as a crucial reagent for chemists seeking to innovate in drug discovery and development, offering a reliable pathway to create diverse chemical entities with potential therapeutic benefits.

Synonyms
Ácido 2-etoxibencenoborónico
CAS Number
213211-69-9
Purity
≥ 95% (Ensayo por titulación)
Molecular Formula
C8H11BO3
Molecular Weight
165.98
MDL Number
MFCD00674027
PubChem ID
2734902
Melting Point
103 °C (Literatura)
Appearance
Polvo cristalino de color blanco a amarillo claro.
Conditions
Tienda en RT
General Information
Synonyms
Ácido 2-etoxibencenoborónico
CAS Number
213211-69-9
Purity
≥ 95% (Ensayo por titulación)
Molecular Formula
C8H11BO3
Molecular Weight
165.98
MDL Number
MFCD00674027
PubChem ID
2734902
Melting Point
103 °C (Literatura)
Appearance
Polvo cristalino de color blanco a amarillo claro.
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-Ethoxyphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key reagent in Suzuki-Miyaura cross-coupling reactions, allowing chemists to create complex organic molecules efficiently.
  • Pharmaceutical Development: It plays a crucial role in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting cancer and other diseases.
  • Material Science: Used in the production of advanced materials, including polymers and nanomaterials, enhancing their properties for applications in electronics and coatings.
  • Bioconjugation: The compound is valuable for attaching biomolecules to surfaces or other molecules, facilitating research in biochemistry and molecular biology.
  • Analytical Chemistry: It is employed in the development of sensors and analytical methods for detecting specific compounds, improving accuracy and sensitivity in various assays.

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