Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
28458
CAS Number:
123324-71-0
4-tert-Butylphenylboronic acid
Purity:
≥ 98% (HPLC)
Synonym(s):
p-tert-Butylbenzeneboronic acid
Documents
$18.53 /5G
Pack Size Availability Price
Request Bulk Quote
Product Information

4-tert-Butylphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. Known for its unique ability to form stable complexes with various substrates, this boronic acid derivative serves as a crucial building block in the development of pharmaceuticals and agrochemicals. Its distinctive tert-butyl group enhances solubility and stability, making it particularly valuable in reactions such as Suzuki coupling, which is essential for constructing complex organic molecules. Researchers appreciate its efficiency in facilitating cross-coupling reactions, leading to the synthesis of biologically active compounds and advanced materials.

In addition to its applications in synthetic chemistry, 4-tert-Butylphenylboronic acid has shown promise in the development of sensors and materials for drug delivery systems. Its ability to selectively bind to diols and other functional groups allows for the design of innovative platforms in biochemistry and nanotechnology. With its favorable properties and broad applicability, this compound is an excellent choice for researchers and industry professionals looking to enhance their synthetic methodologies and product development.

Synonyms
p-tert-Butylbenzeneboronic acid
CAS Number
123324-71-0
Purity
≥ 98% (HPLC)
Molecular Formula
C10H15BO2
Molecular Weight
178.04
MDL Number
MFCD01009697
PubChem ID
2734320
Melting Point
191-196 °C
Appearance
White to light yellow solid
Conditions
Store at 0-8 °C
General Information
Synonyms
p-tert-Butylbenzeneboronic acid
CAS Number
123324-71-0
Purity
≥ 98% (HPLC)
Molecular Formula
C10H15BO2
Molecular Weight
178.04
MDL Number
MFCD01009697
PubChem ID
2734320
Melting Point
191-196 °C
Appearance
White to light yellow solid
Conditions
Store at 0-8 °C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-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, allowing chemists to create complex organic molecules efficiently. Its stability and reactivity make it a preferred choice for building diverse carbon frameworks.
  • Pharmaceutical Development: In the pharmaceutical industry, it is employed in the synthesis of biologically active compounds, particularly in the development of anti-cancer drugs. Its ability to form stable complexes with various substrates enhances the efficacy of drug candidates.
  • Material Science: This chemical is used in the production of advanced materials, such as polymers and nanomaterials. Its boronic acid functionality allows for the formation of dynamic covalent bonds, which can improve material properties like strength and flexibility.
  • Bioconjugation: Researchers utilize it for bioconjugation processes, where it helps attach biomolecules to surfaces or other molecules. This application is crucial in developing biosensors and targeted drug delivery systems.
  • Environmental Chemistry: It plays a role in environmental monitoring, particularly in detecting and quantifying phenolic compounds in water samples. Its sensitivity and specificity make it an effective tool for ensuring water quality.

Citations