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Catalog Number:
28643
CAS Number:
209919-30-2
4-Chloro-2-methylphenylboronic acid
Purity:
≥ 98%
Synonym(s):
4-Chloro-o-tolueneboronic acid
Documents
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Product Information

4-Chloro-2-methylphenylboronic 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 synthesize a variety of biaryl compounds, which are crucial in the development of pharmaceuticals and agrochemicals. Its application extends to the creation of advanced materials and in the field of sensor technology, where it plays a role in detecting specific biomolecules.

The compound's stability and reactivity make it a preferred choice for chemists looking to enhance reaction efficiency and yield. Its ability to selectively bind to certain substrates allows for targeted modifications in complex molecular structures, thus streamlining the synthesis process. With its broad range of applications, 4-Chloro-2-methylphenylboronic acid stands out as a valuable tool in both research and industrial settings, offering significant advantages over similar compounds in terms of reactivity and specificity.

Synonyms
4-Chloro-o-tolueneboronic acid
CAS Number
209919-30-2
Purity
≥ 98%
Molecular Formula
C7H8BClO2
Molecular Weight
170.4
MDL Number
MFCD02683107
PubChem ID
5017600
Appearance
White Powder
Conditions
Store at 0-8°C
General Information
Synonyms
4-Chloro-o-tolueneboronic acid
CAS Number
209919-30-2
Purity
≥ 98%
Molecular Formula
C7H8BClO2
Molecular Weight
170.4
MDL Number
MFCD02683107
PubChem ID
5017600
Appearance
White Powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-Chloro-2-methylphenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key intermediate in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals. Its boronic acid functionality allows for versatile coupling reactions, enhancing the efficiency of chemical synthesis.
  • Drug Development: In medicinal chemistry, it is used to create compounds with potential therapeutic effects. Its ability to form stable complexes with biomolecules makes it valuable in the design of targeted drug delivery systems.
  • Materials Science: The compound is employed in the development of advanced materials, such as polymers and nanomaterials. Its unique properties facilitate the creation of materials with enhanced mechanical and thermal characteristics.
  • Bioconjugation: It is utilized in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules. This application is crucial in the development of biosensors and diagnostic tools.
  • Chemical Sensors: The compound is also used in the fabrication of chemical sensors due to its ability to selectively bind to specific analytes. This property is beneficial in environmental monitoring and safety applications.

Citations