Discover the new Chem-Impex: Where innovation starts with a bond.

Catalog Number:
31075
CAS Number:
881913-20-8
3-(1-Naphthyl)phenylboronic acid
Purity:
97 - 105% (Assay by titration)
Synonym(s):
3-(1-Naphthyl)benzeneboronic acid
Documents
$84.83 /1G
Pack Size Availability Price
Request Bulk Quote
Product Information

3-(1-Naphthyl)phenylboronic acid is a versatile organoboron compound known for its significant role in organic synthesis and medicinal chemistry. This compound features a unique structure that allows it to act as a crucial building block in the development of pharmaceuticals and agrochemicals. Its ability to form stable complexes with various substrates makes it an invaluable reagent in cross-coupling reactions, particularly in Suzuki-Miyaura coupling, which is widely utilized in the synthesis of complex organic molecules. Researchers appreciate its effectiveness in facilitating the formation of carbon-carbon bonds, thereby streamlining the synthesis of biologically active compounds.

In addition to its synthetic applications, 3-(1-Naphthyl)phenylboronic acid has shown promise in the field of materials science, particularly in the development of sensors and optoelectronic devices. Its unique electronic properties enable it to be used in the fabrication of advanced materials with tailored functionalities. This compound's stability and reactivity make it an attractive choice for researchers looking to innovate in various fields, including drug discovery and materials engineering.

Synonyms
3-(1-Naphthyl)benzeneboronic acid
CAS Number
881913-20-8
Purity
97 - 105% (Assay by titration)
Molecular Formula
C16H13BO2
Molecular Weight
248.09
MDL Number
MFCD11045054
PubChem ID
58881077
Appearance
White to light yellow crystalline powder
Conditions
Store at RT
General Information
Synonyms
3-(1-Naphthyl)benzeneboronic acid
CAS Number
881913-20-8
Purity
97 - 105% (Assay by titration)
Molecular Formula
C16H13BO2
Molecular Weight
248.09
MDL Number
MFCD11045054
PubChem ID
58881077
Appearance
White to light yellow crystalline powder
Conditions
Store at RT
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

3-(1-Naphthyl)phenylboronic acid is widely utilized in research focused on:

  • Organic Synthesis: This compound serves as a key reagent in Suzuki-Miyaura cross-coupling reactions, enabling the formation of carbon-carbon bonds, which is essential for creating complex organic molecules in pharmaceuticals and materials science.
  • Drug Development: Its ability to form stable complexes with various biomolecules makes it valuable in the design of new drugs, particularly in targeting cancer cells and other diseases, enhancing therapeutic efficacy.
  • Sensor Technology: The compound is used in developing sensors for detecting specific biomolecules, offering a sensitive and selective method for monitoring biological processes in medical diagnostics.
  • Polymer Chemistry: It plays a role in the modification of polymers, improving their properties for applications in coatings, adhesives, and other materials, leading to enhanced performance and durability.
  • Environmental Applications: The compound can be utilized in the removal of pollutants from water through boron-based adsorption techniques, contributing to environmental sustainability efforts.

Citations