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Catalog Number:
40140
CAS Number:
342002-80-6
3-(Isopropoxycarbonyl)phenylboronic acid
Purity:
98 - 105% (Assay by titration)
Synonym(s):
3-(Isopropoxycarbonyl)benzeneboronic acid
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Product Information

3-(Isopropoxycarbonyl)phenylboronic 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 the development of various pharmaceuticals and agrochemicals. Its unique structure allows for selective reactions, which are crucial in the synthesis of complex organic molecules. Researchers appreciate its role in Suzuki-Miyaura cross-coupling reactions, where it serves as a key building block for creating biaryl compounds, often found in biologically active molecules.

In addition to its synthetic applications, 3-(Isopropoxycarbonyl)phenylboronic acid is also valuable in materials science, particularly in the development of sensors and polymers. Its ability to interact with biological molecules opens avenues for innovative drug delivery systems and diagnostic tools. The compound's stability and reactivity make it a preferred choice for professionals seeking reliable and efficient solutions in their research and development projects. With its broad range of applications, this compound stands out as a crucial tool for advancing scientific discovery and industrial innovation.

Synonyms
3-(Isopropoxycarbonyl)benzeneboronic acid
CAS Number
342002-80-6
Purity
98 - 105% (Assay by titration)
Molecular Formula
C10H13BO4
Molecular Weight
208.02
MDL Number
MFCD02093047
PubChem ID
2734363
Melting Point
129 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
3-(Isopropoxycarbonyl)benzeneboronic acid
CAS Number
342002-80-6
Purity
98 - 105% (Assay by titration)
Molecular Formula
C10H13BO4
Molecular Weight
208.02
MDL Number
MFCD02093047
PubChem ID
2734363
Melting Point
129 °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-(Isopropoxycarbonyl)phenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound plays a crucial role in synthesizing various pharmaceutical agents, particularly in the development of drugs targeting cancer and diabetes. Its ability to form stable complexes with biomolecules enhances drug efficacy.
  • Organic Synthesis: It serves as an important building block in organic chemistry, facilitating the creation of complex molecules through cross-coupling reactions. This is particularly valuable in the production of fine chemicals and agrochemicals.
  • Material Science: The compound is used in creating advanced materials, including polymers and nanomaterials. Its boronic acid functionality allows for the formation of dynamic covalent bonds, which can improve material properties.
  • Bioconjugation: It is employed in bioconjugation techniques, where it helps attach biomolecules to surfaces or other molecules. This application is significant in developing biosensors and targeted drug delivery systems.
  • Environmental Chemistry: The compound can be utilized in the detection and removal of pollutants, particularly in water treatment processes. Its reactivity with certain contaminants makes it a useful tool for environmental remediation.

Citations