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Catalog Number:
31440
CAS Number:
63503-60-6
3-Chlorophenylboronic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
3-Chlorobenzeneboronic acid, m-Chlorobenzeneboronic acid
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Product Information

3-Chlorophenylboronic 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 create complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals. Its application extends to the synthesis of biologically active compounds, where it plays a crucial role in the formation of carbon-carbon bonds, enhancing the efficiency of synthetic pathways.

Additionally, 3-Chlorophenylboronic acid is valuable in the field of materials science, where it is used to modify surfaces and create functionalized polymers. Its ability to selectively bind to specific substrates allows for the development of advanced materials with tailored properties. This compound stands out due to its ease of handling and compatibility with various reaction conditions, making it a preferred choice for chemists looking to streamline their synthetic processes. Whether in research laboratories or industrial applications, 3-Chlorophenylboronic acid offers significant advantages in efficiency and versatility.

Synonyms
3-Chlorobenzeneboronic acid, m-Chlorobenzeneboronic acid
CAS Number
63503-60-6
Purity
≥ 99% (HPLC)
Molecular Formula
C6H6BClO2
Molecular Weight
156.38
MDL Number
MFCD00161354
PubChem ID
2734323
Melting Point
185 - 189 ?C
Appearance
White to off-white powder
Conditions
Store at RT
General Information
Synonyms
3-Chlorobenzeneboronic acid, m-Chlorobenzeneboronic acid
CAS Number
63503-60-6
Purity
≥ 99% (HPLC)
Molecular Formula
C6H6BClO2
Molecular Weight
156.38
MDL Number
MFCD00161354
PubChem ID
2734323
Melting Point
185 - 189 ?C
Appearance
White to off-white 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-Chlorophenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound plays a crucial role in synthesizing various pharmaceuticals, particularly in the development of drugs targeting cancer and diabetes. Its ability to form stable complexes with certain biomolecules enhances drug efficacy.
  • Organic Synthesis: It serves as a versatile building block in organic chemistry, allowing researchers to create complex molecules through Suzuki coupling reactions. This application is essential in the production of agrochemicals and fine chemicals.
  • Material Science: Used in the development of advanced materials, 3-Chlorophenylboronic acid contributes to the creation of polymers with tailored properties, such as improved conductivity and strength, which are valuable in electronics and coatings.
  • Bioconjugation: This compound is utilized in bioconjugation processes, where it helps attach biomolecules to surfaces or other compounds. This is particularly useful in developing biosensors and targeted drug delivery systems.
  • Research in Chemical Biology: Its application in chemical biology allows scientists to study protein interactions and cellular processes, providing insights that are critical for understanding disease mechanisms and developing new therapeutic strategies.

Citations