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Catalog Number:
28281
CAS Number:
32316-92-0
2-Naphthaleneboronic acid
Purity:
≥ 99% (HPLC)
Documents
$18.53 /5G
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Product Information

2-Naphthaleneboronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. This boronic acid derivative is recognized for its ability to form stable complexes with diols, making it an essential reagent in Suzuki-Miyaura cross-coupling reactions. Its unique properties allow for the development of complex organic molecules, which are crucial in the synthesis of pharmaceuticals and agrochemicals. Researchers appreciate its role in the creation of biologically active compounds, including potential drug candidates, due to its compatibility with various functional groups and ease of handling.

In addition to its applications in synthetic chemistry, 2-Naphthaleneboronic acid is also employed in the development of sensors and materials science, particularly in the design of fluorescent probes for detecting biomolecules. Its ability to selectively bind to certain substrates enhances its utility in diagnostic applications. With its broad range of applications and significant advantages over similar compounds, 2-Naphthaleneboronic acid stands out as a valuable tool for researchers and industry professionals looking to innovate and expand their chemical repertoire.

CAS Number
32316-92-0
Purity
≥ 99% (HPLC)
Molecular Formula
C10H9BO2
Molecular Weight
171.99
MDL Number
MFCD00236051
PubChem ID
2734375
Appearance
White powder
Conditions
Store at 0-8°C
General Information
CAS Number
32316-92-0
Purity
≥ 99% (HPLC)
Molecular Formula
C10H9BO2
Molecular Weight
171.99
MDL Number
MFCD00236051
PubChem ID
2734375
Appearance
White powder
Conditions
Store at 0-8°C
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

2-Naphthaleneboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a versatile building block in the synthesis of complex organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It plays a crucial role in Suzuki-Miyaura coupling reactions, enabling the formation of carbon-carbon bonds, which is essential in creating diverse organic compounds.
  • Fluorescent Probes: Researchers use it to develop fluorescent probes for biochemical applications, enhancing the detection of biomolecules in various assays.
  • Material Science: This chemical is applied in the creation of advanced materials, such as polymers and nanomaterials, which have applications in electronics and sensors.
  • Drug Development: Its ability to form stable complexes with various substrates makes it valuable in drug design, particularly in targeting specific biological pathways.

Citations