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Catalog Number:
40130
CAS Number:
560132-24-3
3-tert-Butylphenylboronic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
3-tert-Butylbenzeneboronic acid
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$54.08 /1G
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Product Information

3-tert-Butylphenylboronic 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 Suzuki-Miyaura cross-coupling reactions. Its unique structure, featuring a tert-butyl group, enhances its solubility and stability in various solvents, which is particularly beneficial for researchers looking to optimize reaction conditions.

In the pharmaceutical industry, 3-tert-Butylphenylboronic acid plays a crucial role in the development of biologically active compounds, including potential drug candidates. Its applications extend to the synthesis of complex organic molecules, where it serves as a building block for creating intricate molecular architectures. With its favorable reactivity and functional group compatibility, this compound is an invaluable tool for chemists aiming to streamline their synthetic pathways and improve yields in their research.

Synonyms
3-tert-Butylbenzeneboronic acid
CAS Number
560132-24-3
Purity
≥ 98% (HPLC)
Molecular Formula
C10H15BO2
Molecular Weight
178.04
MDL Number
MFCD11110647
PubChem ID
21582509
Melting Point
221 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
3-tert-Butylbenzeneboronic acid
CAS Number
560132-24-3
Purity
≥ 98% (HPLC)
Molecular Formula
C10H15BO2
Molecular Weight
178.04
MDL Number
MFCD11110647
PubChem ID
21582509
Melting Point
221 °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

3-tert-Butylphenylboronic 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 pharmaceutical industry for synthesizing complex molecules.
  • Drug Development: Its ability to form stable complexes with biomolecules makes it useful in drug design, particularly for targeting specific proteins or enzymes, enhancing the efficacy of therapeutic agents.
  • Material Science: Employed in the development of advanced materials, such as polymers and nanocomposites, where it contributes to improved mechanical properties and thermal stability.
  • Analytical Chemistry: This compound is used in the preparation of boron-containing sensors, which can detect various analytes with high sensitivity, making it beneficial for environmental monitoring and quality control in manufacturing.
  • Bioconjugation: It plays a role in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other compounds, which is essential in creating targeted drug delivery systems and diagnostic tools.

Citations