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Catalog Number:
26701
CAS Number:
1287753-39-2
[4-(1-Ethoxyethyl)phenyl]boronic acid
Purity:
≥ 96% (NMR)
Documents
$52.88 /100MG
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Product Information

[4-(1-Ethoxyethyl)phenyl]boronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the formation of complex organic molecules. Its unique structure allows for enhanced reactivity and selectivity, which is particularly beneficial in the development of pharmaceuticals and agrochemicals. Researchers appreciate its role in the synthesis of biologically active compounds, including potential drug candidates, due to its compatibility with various functional groups.

In addition to its synthetic applications, [4-(1-ethoxyethyl)phenyl]boronic acid is also employed in the development of sensors and materials science, where its boron functionality can facilitate interactions with biomolecules. This compound stands out for its ease of handling and stability under standard laboratory conditions, making it a preferred choice for both academic and industrial applications. Its potential to streamline synthetic pathways and improve yields positions it as a valuable asset in the toolkit of chemists and researchers alike.

CAS Number
1287753-39-2
Purity
≥ 96% (NMR)
Molecular Formula
C10H15BO3
Molecular Weight
194.04
MDL Number
MFCD08059887
PubChem ID
45791079
Appearance
White powder
Conditions
Store at 0-8°C
General Information
CAS Number
1287753-39-2
Purity
≥ 96% (NMR)
Molecular Formula
C10H15BO3
Molecular Weight
194.04
MDL Number
MFCD08059887
PubChem ID
45791079
Appearance
White powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

[4-(1-Ethoxyethyl)phenyl]boronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Medicinal Chemistry: It is employed in drug discovery processes, especially for creating compounds that target specific biological pathways, enhancing the efficacy of therapeutic agents.
  • Bioconjugation: The unique properties of this boronic acid allow for effective bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other compounds for diagnostic and therapeutic applications.
  • Material Science: It is used in the development of advanced materials, including polymers and nanomaterials, which can improve the performance of electronic devices and sensors.
  • Chemical Sensors: The compound can be integrated into chemical sensors for detecting specific analytes, offering high sensitivity and selectivity in various environmental and biomedical applications.

Citations