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Catalog Number:
40091
CAS Number:
190661-29-1
Ácido 2-benciloxifenilborónico
Purity:
≥ 98% (Ensayo por titulación)
Synonym(s):
Ácido 2-benciloxibencenoborónico
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$18.50 /1G
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Product Information

2-Benzyloxyphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form reversible covalent bonds with diols, making it an essential reagent in the development of various pharmaceuticals and agrochemicals. Its unique structure allows for selective binding, which is particularly valuable in the synthesis of complex molecules, including those used in drug discovery and development. Researchers appreciate its role in Suzuki-Miyaura cross-coupling reactions, where it facilitates the formation of carbon-carbon bonds, thereby streamlining the synthesis of biologically active compounds.

In addition to its applications in synthetic chemistry, 2-Benzyloxyphenylboronic acid has shown promise in the field of materials science, particularly in the development of sensors and catalysts. Its ability to interact with biological molecules also opens avenues for potential therapeutic applications, including targeted drug delivery systems. With its favorable reactivity and functional versatility, this compound stands out as a valuable tool for researchers and industry professionals seeking to innovate in chemical synthesis and materials development.

Synonyms
Ácido 2-benciloxibencenoborónico
CAS Number
190661-29-1
Purity
≥ 98% (Ensayo por titulación)
Molecular Formula
C 13 H 13 BO 3
Molecular Weight
228.05
MDL Number
MFCD01632206
PubChem ID
2773253
Melting Point
105 - 110 °C
Appearance
Polvo blanco
Conditions
Tienda en RT
General Information
Synonyms
Ácido 2-benciloxibencenoborónico
CAS Number
190661-29-1
Purity
≥ 98% (Ensayo por titulación)
Molecular Formula
C 13 H 13 BO 3
Molecular Weight
228.05
MDL Number
MFCD01632206
PubChem ID
2773253
Melting Point
105 - 110 °C
Appearance
Polvo blanco
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-Benzyloxyphenylboronic 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.
  • Cross-Coupling Reactions: It is commonly employed in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds in organic chemistry, facilitating the creation of diverse compounds.
  • Bioconjugation: The compound is useful in bioconjugation processes, allowing researchers to attach biomolecules to surfaces or other molecules, enhancing drug delivery systems and diagnostics.
  • Fluorescent Probes: It can be utilized to create fluorescent probes for biological imaging, helping scientists visualize cellular processes in real-time, which is crucial for drug discovery and development.
  • Material Science: This chemical is applied in the development of advanced materials, such as polymers and nanomaterials, which can be used in electronics, sensors, and energy storage solutions.

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