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Catalog Number:
40146
CAS Number:
121554-09-4
4-n-Octyloxyphenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
4-n-Octyloxybenzeneboronic acid
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Product Information

4-n-Octyloxyphenylboronic acid is a versatile compound known for its unique properties that make it invaluable in various applications, particularly in organic synthesis and materials science. This boronic acid derivative features a long octyloxy chain, enhancing its solubility in organic solvents and making it an excellent candidate for use in liquid crystal displays (LCDs) and organic light-emitting diodes (OLEDs). Its ability to form stable complexes with diols allows it to function effectively as a reagent in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds in the synthesis of complex organic molecules.

Researchers and industry professionals can leverage 4-n-Octyloxyphenylboronic acid in the development of advanced materials, pharmaceuticals, and agrochemicals. Its unique structure not only contributes to improved performance in electronic applications but also provides a pathway for the synthesis of novel compounds with tailored properties. This compound stands out due to its combination of solubility, reactivity, and stability, making it a preferred choice for those looking to innovate in their respective fields.

Synonyms
4-n-Octyloxybenzeneboronic acid
CAS Number
121554-09-4
Purity
97 - 105% (Assay by titration)
Molecular Formula
C14H23BO3
Molecular Weight
250.15
MDL Number
MFCD00982004
PubChem ID
3977284
Melting Point
73 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-n-Octyloxybenzeneboronic acid
CAS Number
121554-09-4
Purity
97 - 105% (Assay by titration)
Molecular Formula
C14H23BO3
Molecular Weight
250.15
MDL Number
MFCD00982004
PubChem ID
3977284
Melting Point
73 °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

4-n-Octyloxyphenylboronic acid is widely utilized in research focused on:

  • Organic Electronics: This compound is used in the development of organic semiconductors, particularly in organic light-emitting diodes (OLEDs) and organic photovoltaics, enhancing device efficiency and stability.
  • Drug Delivery Systems: Its boronic acid functionality allows for the selective binding of sugars, making it useful in designing targeted drug delivery systems that can release therapeutic agents in response to specific biological stimuli.
  • Sensor Technology: The compound is employed in the fabrication of sensors for glucose detection, providing a reliable method for monitoring blood sugar levels in diabetic patients.
  • Chemical Synthesis: It serves as a key reagent in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds in the synthesis of complex organic molecules.
  • Polymer Chemistry: This chemical is incorporated into polymer matrices to enhance mechanical properties and thermal stability, making it valuable in the production of advanced materials for various industrial applications.

Citations