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Catalog Number:
40084
CAS Number:
342002-82-8
4-(Isopropoxycarbonyl)phenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
4-(Isopropoxycarbonyl)benzeneboronic acid
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Product Information

4-(Isopropoxycarbonyl)phenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative features a unique isopropoxycarbonyl group, enhancing its reactivity and making it an essential building block in the development of pharmaceuticals and agrochemicals. Its ability to form stable complexes with diols and other nucleophiles allows for efficient coupling reactions, particularly in the synthesis of complex organic molecules. Researchers appreciate its role in Suzuki-Miyaura cross-coupling reactions, which are pivotal in constructing carbon-carbon bonds, thereby facilitating the creation of diverse chemical libraries.

In addition to its synthetic applications, 4-(Isopropoxycarbonyl)phenylboronic acid has shown promise in the development of targeted therapies, particularly in the field of cancer research. Its selective binding properties can be harnessed to deliver therapeutic agents to specific cellular targets, enhancing treatment efficacy while minimizing side effects. With its unique structural features and practical applications, this compound stands out as a valuable resource for researchers and industry professionals seeking innovative solutions in chemical synthesis and drug development.

Synonyms
4-(Isopropoxycarbonyl)benzeneboronic acid
CAS Number
342002-82-8
Purity
97 - 105% (Assay by titration)
Molecular Formula
C10H13BO4
Molecular Weight
208.02
MDL Number
MFCD02259385
PubChem ID
2734703
Melting Point
111 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-(Isopropoxycarbonyl)benzeneboronic acid
CAS Number
342002-82-8
Purity
97 - 105% (Assay by titration)
Molecular Formula
C10H13BO4
Molecular Weight
208.02
MDL Number
MFCD02259385
PubChem ID
2734703
Melting Point
111 °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-(Isopropoxycarbonyl)phenylboronic acid is widely utilized in research focused on:

  • Drug Development: This compound serves as a key building block in the synthesis of pharmaceuticals, particularly in the development of anti-cancer agents. Its boronic acid functionality allows for the formation of stable complexes with biomolecules, enhancing drug efficacy.
  • Organic Synthesis: It is frequently employed in cross-coupling reactions, such as Suzuki-Miyaura coupling, which is essential for creating complex organic molecules. This application is particularly valuable in the production of agrochemicals and fine chemicals.
  • Material Science: The compound is used in the development of advanced materials, including polymers and nanomaterials. Its unique properties enable the creation of materials with tailored functionalities, suitable for applications in electronics and sensors.
  • Bioconjugation: In biochemistry, it is utilized for labeling biomolecules, aiding in the study of protein interactions and cellular processes. This application is crucial for researchers in the fields of proteomics and molecular biology.
  • Environmental Chemistry: The compound can be applied in the detection and removal of pollutants, particularly in water treatment processes. Its ability to form complexes with heavy metals makes it a valuable tool for environmental remediation efforts.

Citations