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Catalog Number:
40113
CAS Number:
146449-90-3
4-Pentyloxyphenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
4-Pentyloxybenzeneboronic acid, 4-Amyloxyphenylboronic acid, 4-Amyloxybenzeneboronic acid
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Product Information

4-Pentyloxyphenylboronic acid is a versatile compound widely utilized in organic synthesis and materials science. This boronic acid derivative is particularly valued for its ability to form stable complexes with diols, making it an essential reagent in the development of sensors and drug delivery systems. Its unique structure allows for effective incorporation into various organic reactions, including Suzuki coupling, which is crucial for the formation of carbon-carbon bonds in the synthesis of complex organic molecules.

In addition to its synthetic applications, 4-Pentyloxyphenylboronic acid has shown promise in the field of medicinal chemistry, where it can be employed in the design of targeted therapies and diagnostic agents. Researchers appreciate its compatibility with a range of functional groups, enhancing its utility in diverse chemical environments. With its favorable properties and broad applicability, this compound stands out as a valuable tool for professionals in both academic and industrial settings.

Synonyms
4-Pentyloxybenzeneboronic acid, 4-Amyloxyphenylboronic acid, 4-Amyloxybenzeneboronic acid
CAS Number
146449-90-3
Purity
97 - 105% (Assay by titration)
Molecular Formula
C11H17BO3
Molecular Weight
208.06
MDL Number
MFCD04039035
PubChem ID
4684888
Melting Point
80 °C (Lit.)
Appearance
White to orange crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-Pentyloxybenzeneboronic acid, 4-Amyloxyphenylboronic acid, 4-Amyloxybenzeneboronic acid
CAS Number
146449-90-3
Purity
97 - 105% (Assay by titration)
Molecular Formula
C11H17BO3
Molecular Weight
208.06
MDL Number
MFCD04039035
PubChem ID
4684888
Melting Point
80 °C (Lit.)
Appearance
White to orange 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

4-Pentyloxyphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Drug Development: Its boronic acid functionality allows for the formation of reversible covalent bonds with diols, making it useful in designing targeted drug delivery systems.
  • Material Science: It is employed in the creation of advanced materials, such as polymers and hydrogels, which can be tailored for specific applications in biotechnology and electronics.
  • Sensor Technology: The compound is used in the development of chemical sensors due to its ability to selectively bind to certain biomolecules, enhancing detection methods in medical diagnostics.
  • Research on Catalysis: It plays a role in catalytic processes, particularly in cross-coupling reactions, which are essential in synthesizing complex organic compounds efficiently.

Citations