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Catalog Number:
31926
CAS Number:
13922-41-3
Naphthalene-1-boronic acid
Purity:
≥ 99% (HPLC)
Synonym(s):
α-Naphthaleneboronic acid, α-Naphthylboronic acid, 1-Naphthalenyl-boronic acid, 1-Naphthaleneboronic acid
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Product Information

Naphthalene-1-boronic 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 the development of various pharmaceuticals and agrochemicals. Its unique properties enable it to serve as a key building block in the synthesis of biologically active molecules, particularly in the creation of targeted drug delivery systems and in the development of fluorescent probes for biological imaging.

Researchers appreciate Naphthalene-1-boronic acid for its ease of use and compatibility with a variety of reaction conditions, which enhances its appeal in both academic and industrial settings. Its applications extend to the synthesis of polymers and materials science, where it contributes to the development of advanced materials with tailored properties. With its significant role in facilitating complex chemical transformations, Naphthalene-1-boronic acid stands out as a valuable tool for chemists aiming to innovate in their respective fields.

Synonyms
α-Naphthaleneboronic acid, α-Naphthylboronic acid, 1-Naphthalenyl-boronic acid, 1-Naphthaleneboronic acid
CAS Number
13922-41-3
Purity
≥ 99% (HPLC)
Molecular Formula
C10H9BO2
Molecular Weight
171.99
MDL Number
MFCD00019722
PubChem ID
254532
Melting Point
206 - 217 ?C
Appearance
White powder
Conditions
Store at 0-8°C
General Information
Synonyms
α-Naphthaleneboronic acid, α-Naphthylboronic acid, 1-Naphthalenyl-boronic acid, 1-Naphthaleneboronic acid
CAS Number
13922-41-3
Purity
≥ 99% (HPLC)
Molecular Formula
C10H9BO2
Molecular Weight
171.99
MDL Number
MFCD00019722
PubChem ID
254532
Melting Point
206 - 217 ?C
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

Naphthalene-1-boronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key building block in the synthesis of various organic molecules, particularly in the development of pharmaceuticals and agrochemicals.
  • Cross-Coupling Reactions: It is essential in Suzuki-Miyaura coupling reactions, which are crucial for forming carbon-carbon bonds in complex organic compounds, making it valuable in materials science and drug development.
  • Fluorescent Probes: Naphthalene-1-boronic acid is used in creating fluorescent probes for detecting biomolecules, enhancing research in biochemistry and molecular biology.
  • Sensor Development: Its ability to form complexes with sugars makes it useful in developing sensors for glucose and other carbohydrates, benefiting the food industry and medical diagnostics.
  • Polymer Chemistry: This compound is incorporated into polymer formulations to improve properties such as thermal stability and mechanical strength, making it relevant in the production of advanced materials.

Citations