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Catalog Number:
40159
CAS Number:
108238-09-1
2-Phenoxyphenylboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
2-Phenoxybenzeneboronic acid
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Product Information

2-Phenoxyphenylboronic 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 pharmaceutical agents and agrochemicals. Its unique structure allows it to act as a key building block in the synthesis of complex organic molecules, particularly in the formation of carbon-carbon bonds through Suzuki-Miyaura coupling reactions. Researchers have leveraged its properties to enhance the efficacy of drug candidates and improve the selectivity of chemical reactions, showcasing its relevance in both academic and industrial settings.

In addition to its synthetic applications, 2-Phenoxyphenylboronic acid has shown promise in the field of materials science, particularly in the development of functional polymers and sensors. Its ability to interact with biological molecules opens avenues for applications in targeted drug delivery and diagnostic tools. With its favorable reactivity and compatibility with various reaction conditions, this compound stands out as a valuable asset for chemists seeking innovative solutions in their research and development projects.

Synonyms
2-Phenoxybenzeneboronic acid
CAS Number
108238-09-1
Purity
95 - 105% (Assay by titration)
Molecular Formula
C12H11BO3
Molecular Weight
214.03
MDL Number
MFCD01001592
PubChem ID
2773559
Melting Point
114 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
2-Phenoxybenzeneboronic acid
CAS Number
108238-09-1
Purity
95 - 105% (Assay by titration)
Molecular Formula
C12H11BO3
Molecular Weight
214.03
MDL Number
MFCD01001592
PubChem ID
2773559
Melting Point
114 °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-Phenoxyphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds. This is particularly valuable in the synthesis of complex organic molecules, such as pharmaceuticals and agrochemicals.
  • Drug Development: Its ability to form reversible complexes with diols makes it useful in the design of drug delivery systems. Researchers can leverage this property to create targeted therapies that release drugs in specific environments within the body.
  • Material Science: This compound is employed in the development of advanced materials, including sensors and organic light-emitting diodes (OLEDs). Its unique properties enhance the efficiency and performance of these materials.
  • Biochemistry: In biochemical research, it is utilized for the detection and quantification of carbohydrates and other biomolecules, aiding in the study of metabolic processes and disease mechanisms.
  • Environmental Science: The compound can be applied in the development of sensors for detecting pollutants, contributing to environmental monitoring and protection efforts.

Citations