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Catalog Number:
27554
CAS Number:
1679-18-1
Ácido 4-clorofenilborónico
Purity:
≥ 99 % (HPLC)
Synonym(s):
(4-Clorofenil)boranediol
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Product Information

4-Chlorophenylboronic acid is a versatile organoboron compound recognized for its utility in various chemical applications, particularly in organic synthesis and medicinal chemistry. This compound is characterized by its ability to form stable complexes with diols, making it an essential reagent in the development of boronate esters and in Suzuki-Miyaura cross-coupling reactions. Its unique properties enable researchers to explore novel pathways in drug discovery and material science, facilitating the synthesis of complex organic molecules with precision.

In the pharmaceutical industry, 4-Chlorophenylboronic acid serves as a crucial building block for the synthesis of biologically active compounds, including potential therapeutic agents. Its effectiveness in coupling reactions allows for the efficient construction of carbon-carbon bonds, which is vital in the development of new drugs. Additionally, its role in sensor technology and polymer chemistry highlights its broad applicability, making it a valuable asset for researchers and industry professionals seeking innovative solutions in their projects.

Synonyms
(4-Clorofenil)boranediol
CAS Number
1679-18-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C6H6BClO2
Molecular Weight
156.38
MDL Number
MFCD00039137
PubChem ID
74299
Melting Point
256 - 275 ?C
Appearance
Sólido cristalino de color blanco a muy ligero
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
(4-Clorofenil)boranediol
CAS Number
1679-18-1
Purity
≥ 99 % (HPLC)
Molecular Formula
C6H6BClO2
Molecular Weight
156.38
MDL Number
MFCD00039137
PubChem ID
74299
Melting Point
256 - 275 ?C
Appearance
Sólido cristalino de color blanco a muy ligero
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

4-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 in the development of anti-cancer agents due to its ability to form stable complexes with certain biomolecules.
  • Organic Synthesis: It is widely used in Suzuki coupling reactions, which are essential for creating complex organic molecules. This application is crucial in the fields of materials science and organic electronics.
  • Bioconjugation: Researchers leverage its boronic acid functionality to selectively bind carbohydrates, making it valuable in the design of targeted drug delivery systems and diagnostic tools.
  • Sensor Technology: The compound is employed in the development of chemical sensors that detect glucose levels, offering significant benefits in diabetes management and monitoring.
  • Polymer Chemistry: It plays a role in the modification of polymers to enhance their properties, such as conductivity and mechanical strength, which is beneficial in the production of advanced materials.

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