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Catalog Number:
26692
CAS Number:
685514-61-8
Acide 2,3-dihydro-1-benzofuran-7-ylboronique
Purity:
≥ 95 % (RMN)
Documents
$60.39 /100 mg
Taille
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Product Information

2,3-Dihydro-1-benzofuran-7-ylboronic acid is a versatile compound with significant applications in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to participate in Suzuki-Miyaura cross-coupling reactions, making it an essential building block for the synthesis of complex organic molecules, including pharmaceuticals and agrochemicals. Its unique structure, featuring a benzofuran moiety, enhances its reactivity and selectivity in various chemical transformations, which is particularly beneficial for researchers looking to develop new compounds with specific biological activities.

In addition to its synthetic utility, 2,3-Dihydro-1-benzofuran-7-ylboronic acid has shown promise in the development of targeted therapies, especially in oncology and neurology. Its ability to form stable complexes with various substrates allows for the design of innovative drug delivery systems. Researchers and industry professionals can leverage this compound to explore new avenues in drug discovery and development, making it a valuable addition to any chemical toolkit.

CAS Number
685514-61-8
Purity
≥ 95 % (RMN)
Molecular Formula
C 8 H 9 B O 3
Molecular Weight
164.0
MDL Number
MFCD06801700
PubChem ID
16427144
Appearance
Blanc cassé uni
Conditions
Conserver à 0-8°C
General Information
CAS Number
685514-61-8
Purity
≥ 95 % (RMN)
Molecular Formula
C 8 H 9 B O 3
Molecular Weight
164.0
MDL Number
MFCD06801700
PubChem ID
16427144
Appearance
Blanc cassé uni
Conditions
Conserver à 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
Non
Antibiotic
Non
DEA-regulated
Non
Warnings
-
Applications

2,3-Dihydro-1-benzofuran-7-ylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in organic chemistry, facilitating the creation of complex molecules through Suzuki-Miyaura cross-coupling reactions.
  • Pharmaceutical Development: It plays a crucial role in drug discovery, particularly in the development of boron-containing pharmaceuticals, which can enhance the efficacy of therapeutic agents.
  • Material Science: The compound is used in the synthesis of advanced materials, including polymers and nanomaterials, benefiting industries focused on electronics and coatings.
  • Bioconjugation: It is employed in bioconjugation techniques, allowing researchers to attach biomolecules to surfaces or other molecules, which is essential in diagnostics and therapeutic applications.
  • Analytical Chemistry: This chemical is utilized in the development of sensors and probes for detecting specific biomolecules, enhancing the sensitivity and selectivity of analytical methods.

Citations