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Catalog Number:
40196
CAS Number:
328956-61-2
Acide 3-chloro-5-fluorophénylboronique
Purity:
97 - 105 % (dosage par titrage)
Synonym(s):
Acide 3-chloro-5-fluorobenzèneboronique
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Product Information

3-Chloro-5-fluorophenylboronic acid is a versatile organoboron compound known for its significant role in organic synthesis and medicinal chemistry. This compound features a boronic acid functional group, making it particularly valuable in Suzuki coupling reactions, which are essential for the formation of carbon-carbon bonds. Its unique structure, characterized by the presence of both chlorine and fluorine substituents, enhances its reactivity and selectivity in various chemical transformations. Researchers and industry professionals utilize 3-Chloro-5-fluorophenylboronic acid for the development of pharmaceuticals, agrochemicals, and advanced materials, where precise molecular modifications are crucial.

In addition to its applications in synthesis, this compound is also explored for its potential in drug discovery, particularly in the design of targeted therapies. Its ability to form stable complexes with various substrates allows for innovative approaches in the development of new therapeutic agents. With its favorable properties and broad applicability, 3-Chloro-5-fluorophenylboronic acid stands out as a key reagent for those looking to enhance their research and product development efforts.

Synonyms
Acide 3-chloro-5-fluorobenzèneboronique
CAS Number
328956-61-2
Purity
97 - 105 % (dosage par titrage)
Molecular Formula
C6H5BClFO2
Molecular Weight
174.36
MDL Number
MFCD06801741
PubChem ID
15391287
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
General Information
Synonyms
Acide 3-chloro-5-fluorobenzèneboronique
CAS Number
328956-61-2
Purity
97 - 105 % (dosage par titrage)
Molecular Formula
C6H5BClFO2
Molecular Weight
174.36
MDL Number
MFCD06801741
PubChem ID
15391287
Appearance
Poudre cristalline blanche à blanc cassé
Conditions
Magasin chez RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

3-Chloro-5-fluorophenylboronic 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 targeted cancer therapies. Its ability to form stable complexes with biomolecules enhances drug efficacy.
  • Organic Synthesis: It serves as a key building block in the synthesis of complex organic molecules, allowing chemists to create diverse compounds with specific functionalities, which is essential in materials science and agrochemicals.
  • Cross-Coupling Reactions: This chemical is effective in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. This application is vital in producing fine chemicals and intermediates in the chemical industry.
  • Diagnostic Reagents: It is used in the development of diagnostic agents, particularly in imaging techniques. Its unique properties allow for better visualization in medical imaging, aiding in the early detection of diseases.
  • Research in Material Science: The compound is explored for its potential in creating advanced materials, including polymers and nanomaterials, which have applications in electronics and renewable energy technologies.

Citations