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Catalog Number:
40074
CAS Number:
34420-17-2
2-Phenylethylboronic acid
Purity:
≥ 95% (Assay by titration)
Synonym(s):
Phenethylboronic acid
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Product Information

2-Phenylethylboronic acid is a versatile organoboron compound that plays a crucial role in organic synthesis and medicinal chemistry. This compound is recognized for its ability to form stable complexes with various substrates, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Researchers and industry professionals utilize 2-Phenylethylboronic acid for the synthesis of biaryl compounds, which are pivotal in the development of pharmaceuticals and agrochemicals. Its unique properties allow for selective functionalization, enabling the creation of complex molecular architectures with high efficiency.

In addition to its synthetic applications, 2-Phenylethylboronic acid has shown promise in the field of materials science, particularly in the development of boron-containing polymers and nanomaterials. Its compatibility with various reaction conditions and substrates makes it a preferred choice for chemists looking to innovate in drug discovery and material development. With its growing relevance in diverse fields, 2-Phenylethylboronic acid stands out as a valuable tool for advancing research and industrial applications.

Synonyms
Phenethylboronic acid
CAS Number
34420-17-2
Purity
≥ 95% (Assay by titration)
Molecular Formula
C8H11BO2
Molecular Weight
149.98
MDL Number
MFCD01631226
PubChem ID
65389
Melting Point
88 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
Phenethylboronic acid
CAS Number
34420-17-2
Purity
≥ 95% (Assay by titration)
Molecular Formula
C8H11BO2
Molecular Weight
149.98
MDL Number
MFCD01631226
PubChem ID
65389
Melting Point
88 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Phenylethylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It plays a crucial role in Suzuki-Miyaura coupling reactions, enabling the formation of carbon-carbon bonds, which are essential in creating complex organic structures.
  • Bioconjugation: Researchers use it for bioconjugation processes, attaching biomolecules to surfaces or other molecules, which is vital in drug delivery systems and diagnostics.
  • Material Science: The compound is applied in the development of advanced materials, including polymers and nanomaterials, enhancing their properties for various industrial applications.
  • Medicinal Chemistry: It is significant in the design and development of new therapeutic agents, particularly in targeting specific biological pathways, offering potential advantages over traditional compounds.

Citations