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Catalog Number:
26799
CAS Number:
98-80-6
Phenylboronic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
Dihydroxyphenylborane, Phenyl-boranediol
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Product Information

Phenylboronic acid is a versatile compound widely recognized for its utility in organic synthesis and medicinal chemistry. This aromatic boronic acid serves as a crucial building block in the development of pharmaceuticals, agrochemicals, and advanced materials. Its ability to form reversible covalent bonds with diols makes it particularly valuable in the synthesis of complex organic molecules, including glycosylation reactions and the preparation of boronate esters. Researchers appreciate its role in the development of targeted drug delivery systems and in the design of sensors for detecting biomolecules, owing to its selective binding properties.

In addition to its applications in synthetic chemistry, phenylboronic acid is also employed in the production of polymeric materials and in the field of nanotechnology. Its unique reactivity allows for the modification of surfaces and the creation of functionalized nanoparticles, enhancing their performance in various applications. With its broad range of uses, phenylboronic acid stands out as a key compound for researchers and industry professionals seeking innovative solutions in chemical synthesis and material science.

Synonyms
Dihydroxyphenylborane, Phenyl-boranediol
CAS Number
98-80-6
Purity
≥ 99% (HPLC)
Molecular Formula
C6H7BO2
Molecular Weight
121.93
MDL Number
MFCD00002103
PubChem ID
66827
Melting Point
215 - 220 °C
Appearance
White to off-white crystalline powder
Conditions
Store at 0 - 8 °C
General Information
Synonyms
Dihydroxyphenylborane, Phenyl-boranediol
CAS Number
98-80-6
Purity
≥ 99% (HPLC)
Molecular Formula
C6H7BO2
Molecular Weight
121.93
MDL Number
MFCD00002103
PubChem ID
66827
Melting Point
215 - 220 °C
Appearance
White to off-white crystalline powder
Conditions
Store at 0 - 8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

Phenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: It serves as a key reagent in Suzuki-Miyaura cross-coupling reactions, allowing chemists to create complex organic molecules efficiently. This is particularly valuable in pharmaceuticals for developing new drugs.
  • Bioconjugation: Its ability to form reversible covalent bonds with diols makes it useful in bioconjugation techniques, which are essential for creating targeted drug delivery systems and diagnostic tools in the biomedical field.
  • Sensor Development: Phenylboronic acid is employed in the design of glucose sensors, benefiting diabetic patients by providing accurate blood sugar monitoring through its interaction with glucose.
  • Polymer Chemistry: It is used to modify polymers, enhancing their properties for applications in coatings, adhesives, and materials science, leading to improved performance and durability.
  • Environmental Applications: The compound can be utilized in the removal of heavy metals from wastewater, offering a cost-effective solution for industries aiming to reduce their environmental impact.

Citations