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Catalog Number:
40134
CAS Number:
156682-54-1
3-Benzyloxyphenylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
3-Benzyloxybenzeneboronic acid
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Product Information

3-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 stable complexes with diols, making it an essential reagent in the development of various pharmaceuticals and agrochemicals. Its unique structure allows for selective reactions, particularly in Suzuki-Miyaura cross-coupling reactions, which are pivotal in constructing complex organic molecules. Researchers appreciate its role in the synthesis of biologically active compounds, including potential anti-cancer agents and other therapeutic drugs.

In addition to its applications in drug discovery, 3-Benzyloxyphenylboronic acid is also employed in materials science, particularly in the development of sensors and polymers. Its ability to interact with biomolecules enhances its utility in bioconjugation and targeted drug delivery systems. The compound's stability and reactivity make it a preferred choice for researchers looking to streamline their synthetic pathways while achieving high yields. With its broad range of applications, 3-Benzyloxyphenylboronic acid stands out as a valuable tool for professionals in both academic and industrial settings.

Synonyms
3-Benzyloxybenzeneboronic acid
CAS Number
156682-54-1
Purity
95 - 105% (Assay by titration)
Molecular Formula
C13H13BO3
Molecular Weight
228.05
MDL Number
MFCD02093063
PubChem ID
2734313
Melting Point
130 °C (Lit.)
Appearance
White to light yellow crystalline powder
Conditions
Store at RT
General Information
Synonyms
3-Benzyloxybenzeneboronic acid
CAS Number
156682-54-1
Purity
95 - 105% (Assay by titration)
Molecular Formula
C13H13BO3
Molecular Weight
228.05
MDL Number
MFCD02093063
PubChem ID
2734313
Melting Point
130 °C (Lit.)
Appearance
White to light yellow 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

3-Benzyloxyphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key reagent in the Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds, which is essential in creating complex organic molecules.
  • Pharmaceutical Development: It plays a significant role in the synthesis of various pharmaceutical intermediates, aiding in the development of new drugs with improved efficacy and reduced side effects.
  • Materials Science: The compound is used in the modification of polymers and materials, enhancing their properties for applications in electronics and coatings.
  • Bioconjugation: It is employed in bioconjugation techniques, allowing for the attachment of biomolecules to surfaces or other molecules, which is crucial in the development of biosensors and targeted drug delivery systems.
  • Analytical Chemistry: This chemical is utilized in the preparation of boron-containing compounds for analytical methods, improving the detection and quantification of various substances in complex mixtures.

Citations