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Catalog Number:
26707
CAS Number:
219834-95-4
Ácido (4-metoxi-1-naftil)borónico
Purity:
95 - 100 % (LCMS)
Documents
$58.69 /100 mg
Tamaño
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Product Information

(4-Methoxy-1-naphthyl)boronic acid is a versatile compound widely utilized in organic synthesis and medicinal chemistry. Known for its unique boronic acid functionality, this compound serves as a crucial building block in the development of pharmaceuticals and agrochemicals. Its ability to form reversible covalent bonds with diols makes it an essential reagent in Suzuki-Miyaura cross-coupling reactions, facilitating the formation of carbon-carbon bonds. This property is particularly valuable in the synthesis of complex organic molecules, including biologically active compounds and materials for organic electronics.

In addition to its synthetic applications, (4-Methoxy-1-naphthyl)boronic acid has shown promise in the field of sensor technology, where it can be employed in the detection of sugars and other biomolecules. Its stability and reactivity make it a preferred choice for researchers looking to explore new avenues in drug discovery and material science. With its broad range of applications, this compound stands out as a key player in advancing research and development across various scientific disciplines.

CAS Number
219834-95-4
Purity
95 - 100 % (LCMS)
Molecular Formula
C 11 H 11 BO 3
Molecular Weight
202.0
MDL Number
MFCD03452757
PubChem ID
4198749
Melting Point
191 - 195 ?C
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
General Information
CAS Number
219834-95-4
Purity
95 - 100 % (LCMS)
Molecular Formula
C 11 H 11 BO 3
Molecular Weight
202.0
MDL Number
MFCD03452757
PubChem ID
4198749
Melting Point
191 - 195 ?C
Appearance
Polvo de color blanco a blanquecino
Conditions
Conservar entre 0 y 8 °C.
Properties
Additional property information coming soon!
-
Safety and Regulations
Hazmat
No
Antibiotic
No
DEA-regulated
No
Warnings
-
Applications

(4-Methoxy-1-naphthyl)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 frequently used in Suzuki-Miyaura coupling reactions, allowing for the formation of carbon-carbon bonds, which is essential in creating complex organic structures.
  • Fluorescent Probes: The compound can be employed to design fluorescent probes for biological imaging, providing researchers with tools to visualize cellular processes in real-time.
  • Sensor Development: Its boronic acid functionality makes it suitable for developing sensors that detect glucose and other biomolecules, which is particularly beneficial in medical diagnostics.
  • Material Science: In polymer chemistry, it is used to modify polymer properties, enhancing materials for applications in electronics and coatings.

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