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Catalog Number:
40071
CAS Number:
4433-63-0
Ácido etilborónico
Purity:
97 - 105% (Ensayo por titulación)
Synonym(s):
Ácido etanoborónico
Documents
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Product Information

Ethylboronic acid is a versatile organoboron compound known for its significant role in organic synthesis and medicinal chemistry. This compound features a boron atom bonded to an ethyl group and a hydroxyl group, making it an essential reagent in various chemical reactions, particularly in Suzuki-Miyaura cross-coupling reactions. Its ability to form stable complexes with various substrates allows for the efficient synthesis of biaryl compounds, which are crucial in the development of pharmaceuticals, agrochemicals, and advanced materials. Researchers appreciate ethylboronic acid for its ease of handling and compatibility with a wide range of functional groups, making it a preferred choice for chemists looking to streamline their synthetic pathways.

In addition to its synthetic applications, ethylboronic acid has shown promise in the field of diagnostics and sensor development due to its ability to selectively bind to certain biomolecules. This property opens avenues for its use in creating innovative biosensors and diagnostic tools, enhancing the detection of specific analytes in complex biological samples. With its unique features and broad applicability, ethylboronic acid stands out as a valuable compound for both research and industrial applications.

Synonyms
Ácido etanoborónico
CAS Number
4433-63-0
Purity
97 - 105% (Ensayo por titulación)
Molecular Formula
C2H7BO2
Molecular Weight
73.89
MDL Number
MFCD01074536
PubChem ID
521157
Melting Point
84 - 88 °C
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Conservar a ≤ -10 °C
General Information
Synonyms
Ácido etanoborónico
CAS Number
4433-63-0
Purity
97 - 105% (Ensayo por titulación)
Molecular Formula
C2H7BO2
Molecular Weight
73.89
MDL Number
MFCD01074536
PubChem ID
521157
Melting Point
84 - 88 °C
Appearance
Polvo cristalino de color blanco a blanquecino.
Conditions
Conservar a ≤ -10 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Ethylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key building block in the synthesis of various organic molecules, particularly in the formation of carbon-carbon bonds through Suzuki coupling reactions. This makes it invaluable for creating complex pharmaceuticals and agrochemicals.
  • Medicinal Chemistry: Ethylboronic acid is used in the development of boron-containing drugs, which can exhibit unique biological activities. Its ability to form stable complexes with certain biomolecules enhances drug efficacy and selectivity.
  • Material Science: In the production of boron-doped materials, this compound plays a crucial role. It can improve the electrical properties of polymers and semiconductors, making it useful in electronics and energy storage applications.
  • Analytical Chemistry: Ethylboronic acid is employed as a reagent in various analytical techniques, including chromatography and mass spectrometry. It helps in the detection and quantification of certain biomolecules, aiding in research and diagnostics.
  • Environmental Applications: This compound can be utilized in the remediation of contaminated sites. Its ability to form stable complexes with heavy metals allows for the development of methods to extract and remove pollutants from soil and water.

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