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

Catalog Number:
40322
CAS Number:
136496-72-5
4-Carboxy-3-chlorophenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
4-Carboxy-3-chlorobenzeneboronic acid
Documents
$145.52 /1G
Pack Size Availability Price
Request Bulk Quote
Product Information

4-Carboxy-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 the development of various pharmaceuticals and agrochemicals. Its unique properties allow it to serve as a key building block in the synthesis of biologically active compounds, particularly in the creation of targeted therapies for cancer and other diseases. Researchers appreciate its role in Suzuki coupling reactions, which are crucial for constructing complex organic molecules with precision.

In addition to its applications in drug development, 4-Carboxy-3-chlorophenylboronic acid is also valuable in materials science, particularly in the design of sensors and polymers. Its ability to interact with different functional groups enhances its utility in creating innovative materials with tailored properties. The compound's stability and reactivity make it a preferred choice for researchers looking to streamline their synthesis processes while achieving high yields. With its broad range of applications, this compound stands out as a significant tool for professionals in both the pharmaceutical and materials industries.

Synonyms
4-Carboxy-3-chlorobenzeneboronic acid
CAS Number
136496-72-5
Purity
97 - 105% (Assay by titration)
Molecular Formula
C7H6BClO4
Molecular Weight
200.38
MDL Number
MFCD06656268
PubChem ID
14903223
Melting Point
232 °C (dec.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-Carboxy-3-chlorobenzeneboronic acid
CAS Number
136496-72-5
Purity
97 - 105% (Assay by titration)
Molecular Formula
C7H6BClO4
Molecular Weight
200.38
MDL Number
MFCD06656268
PubChem ID
14903223
Melting Point
232 °C (dec.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Carboxy-3-chlorophenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly those targeting cancer and diabetes, due to its ability to form stable complexes with biomolecules.
  • Bioconjugation: It is employed in bioconjugation processes, allowing researchers to attach drugs or imaging agents to proteins, enhancing their therapeutic efficacy and diagnostic capabilities.
  • Material Science: The compound is used in the development of advanced materials, such as sensors and polymers, where its boronic acid functionality can form dynamic covalent bonds, leading to innovative applications in electronics.
  • Organic Synthesis: It plays a significant role in organic synthesis as a reagent for Suzuki-Miyaura coupling reactions, which are vital for constructing complex organic molecules in a more efficient manner.
  • Environmental Monitoring: This chemical is also applied in environmental science for detecting and quantifying phenolic compounds in water samples, contributing to pollution control and environmental safety.

Citations