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Catalog Number:
40081
CAS Number:
16152-51-5
4-Isopropylphenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
4-Isopropylbenzeneboronic acid
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Product Information

4-Isopropylphenylboronic 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. Researchers and industry professionals leverage its unique properties to facilitate the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals. Its effectiveness in catalyzing reactions allows for the efficient construction of carbon-carbon bonds, which is crucial in the creation of various biologically active compounds.

Additionally, 4-Isopropylphenylboronic acid serves as a valuable tool in the field of materials science, where it can be employed in the development of functionalized polymers and advanced materials. Its compatibility with various substrates and ease of handling make it an attractive choice for researchers looking to enhance their synthetic methodologies. With its broad range of applications and significant advantages over similar compounds, 4-Isopropylphenylboronic acid is a key ingredient for innovative research and development in multiple industries.

Synonyms
4-Isopropylbenzeneboronic acid
CAS Number
16152-51-5
Purity
97 - 105% (Assay by titration)
Molecular Formula
C9H13BO2
Molecular Weight
164.01
MDL Number
MFCD01074614
PubChem ID
2773480
Melting Point
140 °C (Lit.)
Appearance
White to light yellow crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-Isopropylbenzeneboronic acid
CAS Number
16152-51-5
Purity
97 - 105% (Assay by titration)
Molecular Formula
C9H13BO2
Molecular Weight
164.01
MDL Number
MFCD01074614
PubChem ID
2773480
Melting Point
140 °C (Lit.)
Appearance
White to light yellow 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-Isopropylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key reagent in the Suzuki coupling reaction, allowing chemists to create complex organic molecules efficiently. Its ability to form stable complexes with various substrates makes it invaluable in developing pharmaceuticals and agrochemicals.
  • Drug Development: In medicinal chemistry, it aids in the design of boron-containing compounds that can enhance the efficacy of drugs. Its unique properties can improve the bioavailability and selectivity of therapeutic agents.
  • Material Science: The compound is used in the development of advanced materials, including polymers and nanomaterials. Its boronic acid functionality allows for the formation of dynamic covalent bonds, which can be exploited in creating smart materials.
  • Bioconjugation: It plays a significant role in bioconjugation techniques, where it is used to attach biomolecules to surfaces or other molecules. This is particularly useful in the development of biosensors and targeted drug delivery systems.
  • Environmental Applications: The compound is also explored for its potential in environmental chemistry, particularly in the detection and removal of pollutants. Its ability to form complexes with certain heavy metals can be harnessed for environmental remediation efforts.

Citations