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Catalog Number:
40085
CAS Number:
352525-98-5
6-Ethoxy-2-naphthaleneboronic acid
Purity:
95 - 105% (Assay by titration)
Documents
$45.37 /1G
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Product Information

6-Ethoxy-2-naphthaleneboronic acid is a versatile boronic acid derivative known for its significant role in organic synthesis and medicinal chemistry. This compound features a unique ethoxy group that enhances its solubility and reactivity, making it an excellent candidate for cross-coupling reactions, particularly in the development of pharmaceuticals and agrochemicals. Its ability to form stable complexes with various substrates allows researchers to explore innovative pathways in drug discovery and material science.

In addition to its synthetic applications, 6-Ethoxy-2-naphthaleneboronic acid is recognized for its potential in the development of fluorescent probes and sensors, providing valuable insights in biological studies. Its compatibility with various reaction conditions and functional groups makes it a preferred choice among chemists looking to streamline their synthetic processes. With its robust performance and adaptability, this compound stands out as a key player in advancing research and industrial applications.

CAS Number
352525-98-5
Purity
95 - 105% (Assay by titration)
Molecular Formula
C12H13BO3
Molecular Weight
216.04
MDL Number
MFCD03427009
PubChem ID
4641693
Melting Point
255 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
CAS Number
352525-98-5
Purity
95 - 105% (Assay by titration)
Molecular Formula
C12H13BO3
Molecular Weight
216.04
MDL Number
MFCD03427009
PubChem ID
4641693
Melting Point
255 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
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Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

6-Ethoxy-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 pharmaceutical industry where it aids in developing new drugs.
  • Cross-Coupling Reactions: It is commonly used in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds, making it invaluable in materials science and organic electronics.
  • Fluorescent Probes: The compound can be employed in creating fluorescent probes for biological imaging, allowing researchers to visualize cellular processes with high specificity.
  • Bioconjugation: It plays a role in bioconjugation chemistry, facilitating the attachment of biomolecules to surfaces or other molecules, which is crucial in developing targeted drug delivery systems.
  • Environmental Applications: This chemical can be used in the detection and removal of pollutants, contributing to environmental monitoring efforts and the development of greener technologies.

Citations