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

Catalog Number:
40154
CAS Number:
153624-46-5
4-Isopropoxyphenylboronic acid
Purity:
≥ 99.5% (HPLC)
Synonym(s):
4-Isopropoxybenzeneboronic acid
Documents
$18.50 /5G
Pack Size Availability Price
Request Bulk Quote
Product Information

4-Isopropoxyphenylboronic acid is a versatile compound widely recognized for its utility in organic synthesis and medicinal chemistry. This boronic acid derivative features a unique isopropoxy group that enhances its reactivity and solubility, making it an ideal candidate for various applications. It is particularly valuable in Suzuki-Miyaura cross-coupling reactions, which are essential for the formation of carbon-carbon bonds in the synthesis of complex organic molecules. Researchers and industry professionals utilize this compound in the development of pharmaceuticals, agrochemicals, and advanced materials, where precision and efficiency are paramount.

Additionally, 4-Isopropoxyphenylboronic acid serves as a crucial building block in the synthesis of biologically active compounds, enabling the creation of novel therapeutic agents. Its ability to form stable complexes with diols makes it useful in sensing applications and in the design of drug delivery systems. With its favorable properties and broad applicability, this compound stands out as a key resource for those engaged in cutting-edge research and development.

Synonyms
4-Isopropoxybenzeneboronic acid
CAS Number
153624-46-5
Purity
≥ 99.5% (HPLC)
Molecular Formula
C9H13BO3
Molecular Weight
180.01
MDL Number
MFCD03427051
PubChem ID
3698726
Melting Point
150 - 154 °C
Appearance
Off-white powder
Conditions
Store at RT
General Information
Synonyms
4-Isopropoxybenzeneboronic acid
CAS Number
153624-46-5
Purity
≥ 99.5% (HPLC)
Molecular Formula
C9H13BO3
Molecular Weight
180.01
MDL Number
MFCD03427051
PubChem ID
3698726
Melting Point
150 - 154 °C
Appearance
Off-white powder
Conditions
Store at RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

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

  • Organic Synthesis: This compound serves as a key intermediate in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Drug Development: Its unique boronic acid functionality allows it to form reversible covalent bonds with diols, making it valuable in designing targeted drug delivery systems and enhancing the efficacy of certain medications.
  • Materials Science: It is used in the creation of advanced materials, including polymers and nanocomposites, which can exhibit improved mechanical properties and thermal stability.
  • Bioconjugation: The compound is employed in bioconjugation techniques, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in diagnostics and therapeutic applications.
  • Environmental Monitoring: Its properties make it suitable for developing sensors that detect environmental pollutants, contributing to efforts in environmental protection and sustainability.

Citations