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Catalog Number:
40087
CAS Number:
103986-53-4
4-Methyl-1-naphthaleneboronic acid
Purity:
95 - 105% (Assay by titration)
Synonym(s):
4-Methyl-1-naphthylboronic acid
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Product Information

4-Methyl-1-naphthaleneboronic acid is a versatile organoboron compound recognized for its significant role in organic synthesis and medicinal chemistry. This compound features a naphthalene backbone with a boronic acid functional group, making it an essential building block for the development of pharmaceuticals and agrochemicals. Its unique properties allow for the formation of stable complexes with various substrates, facilitating cross-coupling reactions such as Suzuki-Miyaura coupling, which is pivotal in constructing complex organic molecules. Researchers and industry professionals utilize 4-Methyl-1-naphthaleneboronic acid in the synthesis of biologically active compounds, including potential drug candidates and advanced materials.

The compound's ability to act as a versatile reagent in organic transformations enhances its appeal in both academic and industrial settings. Its compatibility with a range of functional groups and solvents allows for diverse applications, from the synthesis of fluorescent dyes to the development of novel therapeutic agents. With its proven efficacy and broad applicability, 4-Methyl-1-naphthaleneboronic acid stands out as a valuable asset for researchers aiming to innovate in the fields of chemistry and materials science.

Synonyms
4-Methyl-1-naphthylboronic acid
CAS Number
103986-53-4
Purity
95 - 105% (Assay by titration)
Molecular Formula
C11H11BO2
Molecular Weight
186.02
MDL Number
MFCD01632204
PubChem ID
2773511
Melting Point
207 °C (Lit.)
Appearance
White to off-white crystalline powder
Conditions
Store at RT
General Information
Synonyms
4-Methyl-1-naphthylboronic acid
CAS Number
103986-53-4
Purity
95 - 105% (Assay by titration)
Molecular Formula
C11H11BO2
Molecular Weight
186.02
MDL Number
MFCD01632204
PubChem ID
2773511
Melting Point
207 °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

4-Methyl-1-naphthaleneboronic 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 commonly used in Suzuki-Miyaura coupling reactions, which are essential for forming carbon-carbon bonds in complex organic compounds, making it invaluable in drug discovery.
  • Fluorescent Probes: The compound can be utilized to create fluorescent probes for biological imaging, aiding researchers in tracking cellular processes and understanding disease mechanisms.
  • Material Science: It plays a role in the development of advanced materials, such as conductive polymers and organic light-emitting diodes (OLEDs), enhancing the performance of electronic devices.
  • Chemical Sensors: 4-Methyl-1-naphthaleneboronic acid is used in the fabrication of chemical sensors for detecting specific biomolecules, providing solutions for environmental monitoring and medical diagnostics.

Citations