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Catalog Number:
26262
CAS Number:
913835-76-4
Ácido 4-cloro-2-formilfenilborónico
Purity:
≥ 99 % (HPLC)
Synonym(s):
Ácido 4-cloro-2-formilbencenoborónico, 2-Borono-5-clorobenzaldehído
Documents
$79.22 /250 mg
Tamaño
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Product Information

4-Chloro-2-formylphenylboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative features a chloro substituent and a formyl group, making it an essential building block for the development of various pharmaceuticals and agrochemicals. Its unique reactivity allows for the formation of carbon-carbon bonds through Suzuki-Miyaura coupling reactions, which are crucial in the synthesis of complex organic molecules. Researchers appreciate its ability to facilitate the construction of diverse molecular architectures, thereby enhancing the efficiency of drug discovery processes.

In addition to its synthetic applications, 4-Chloro-2-formylphenylboronic acid has shown potential in the development of targeted therapies, particularly in the field of cancer research. Its boronic acid functionality enables it to interact selectively with biological targets, paving the way for innovative therapeutic strategies. With its robust performance in various chemical reactions and its relevance in cutting-edge research, this compound stands out as a valuable asset for chemists and industry professionals alike.

Synonyms
Ácido 4-cloro-2-formilbencenoborónico, 2-Borono-5-clorobenzaldehído
CAS Number
913835-76-4
Purity
≥ 99 % (HPLC)
Molecular Formula
C7H6BClO3
Molecular Weight
184.39
MDL Number
MFCD08689492
PubChem ID
23730425
Melting Point
132-134 ?C
Appearance
Polvo de color blanquecino a amarillo claro
Conditions
Conservar entre 0 y 8 °C.
General Information
Synonyms
Ácido 4-cloro-2-formilbencenoborónico, 2-Borono-5-clorobenzaldehído
CAS Number
913835-76-4
Purity
≥ 99 % (HPLC)
Molecular Formula
C7H6BClO3
Molecular Weight
184.39
MDL Number
MFCD08689492
PubChem ID
23730425
Melting Point
132-134 ?C
Appearance
Polvo de color blanquecino a amarillo claro
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-Chloro-2-formylphenylboronic acid is widely utilized in research focused on:

  • Synthetic Chemistry: This compound serves as a crucial building block in the synthesis of various organic molecules, enabling chemists to create complex structures efficiently.
  • Pharmaceutical Development: It is employed in the development of new drugs, particularly in creating compounds that target specific biological pathways, enhancing therapeutic efficacy.
  • Material Science: The compound is used in the formulation of advanced materials, such as polymers and nanomaterials, which can exhibit unique properties for applications in electronics and coatings.
  • Bioconjugation: It plays a significant role in bioconjugation processes, facilitating the attachment of biomolecules to surfaces or other molecules, which is essential in diagnostics and therapeutic applications.
  • Environmental Chemistry: Researchers utilize this compound in studies related to environmental remediation, particularly in developing methods to detect and remove pollutants from water sources.

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