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Catalog Number:
40233
CAS Number:
957061-11-9
2-Chloro-3-(trifluoromethyl)phenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
2-Chloro-3-(trifluoromethyl)benzeneboronic acid
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$116.67 /200MG
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Product Information

2-Chloro-3-(trifluoromethyl)phenylboronic acid is a versatile boronic acid derivative known for its significant role in organic synthesis and medicinal chemistry. This compound features a trifluoromethyl group, which enhances its reactivity and selectivity in various chemical reactions, making it an essential building block for the development of pharmaceuticals and agrochemicals. Its unique properties allow it to participate in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds that are crucial in the synthesis of complex organic molecules.

Researchers and industry professionals can leverage 2-Chloro-3-(trifluoromethyl)phenylboronic acid in the design of novel compounds with potential applications in drug discovery and materials science. Its ability to form stable complexes with various substrates opens up avenues for the development of targeted therapies and advanced materials. With its high reactivity and specificity, this compound stands out as a valuable tool in both academic research and industrial applications, offering significant advantages over similar boronic acids in terms of efficiency and effectiveness.

Synonyms
2-Chloro-3-(trifluoromethyl)benzeneboronic acid
CAS Number
957061-11-9
Purity
97 - 105% (Assay by titration)
Molecular Formula
C7H5BClF3O2
Molecular Weight
224.37
MDL Number
MFCD09258745
PubChem ID
44558143
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
2-Chloro-3-(trifluoromethyl)benzeneboronic acid
CAS Number
957061-11-9
Purity
97 - 105% (Assay by titration)
Molecular Formula
C7H5BClF3O2
Molecular Weight
224.37
MDL Number
MFCD09258745
PubChem ID
44558143
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

2-Chloro-3-(trifluoromethyl)phenylboronic acid is widely utilized in research focused on:

  • Pharmaceutical Development: This compound serves as a key intermediate in the synthesis of various pharmaceuticals, particularly in the development of drugs targeting cancer and other diseases.
  • Organic Synthesis: It is employed in cross-coupling reactions, such as Suzuki-Miyaura reactions, allowing chemists to create complex organic molecules efficiently.
  • Material Science: The compound is used in the formulation of advanced materials, including polymers and coatings, enhancing their properties like durability and resistance to environmental factors.
  • Agricultural Chemistry: It plays a role in the development of agrochemicals, contributing to the creation of effective herbicides and pesticides that improve crop yields.
  • Analytical Chemistry: This boronic acid derivative is utilized in sensor technology for detecting specific biomolecules, providing a reliable method for monitoring environmental and biological samples.

Citations