Introduction of CAS:62012-54-8 | 2-bromo-1-methoxynaphthalene
The physical and chemical properties of 2-bromo-6-methoxynaphthalene have been studied extensively. The compound's vibrational, electronic, and charge transfer properties were investigated using DFT methods, revealing an energy gap of 4.208 eV, which indicates molecular stability. The reactive sites of the molecule were predicted using various computational techniques, and the compound was found to exhibit anti-cancer activities, suggesting its potential as a pharmaceutical product . Additionally, the compound's fluorescence properties have been utilized in the development of analytical methods for the detection of biologically active carboxylic acids .
Specification of CAS:62012-54-8 | 2-bromo-1-methoxynaphthalene
|
ITEMS |
SPECIFICATION |
|
Boiling point |
161 °C(Press: 14 Torr) |
|
Density |
1.447±0.06 g/cm3(Predicted) |
|
Form |
light sensitive liquid |
|
Color |
Clear brown |
Research Application of CAS:62012-54-8 | 2-bromo-1-methoxynaphthalene
Application Summary: 2-Bromo-1-methoxynaphthalene is used as a reagent to synthesize a catalyst for highly enantioselective aziridination of styrene derivatives .
Methods of Application: The specific experimental procedures and technical details may vary, but generally, this involves the reaction of 2-Bromo-1-methoxynaphthalene with styrene derivatives in the presence of a catalyst . The process is typically carried out under controlled conditions in a laboratory setting.
Results or Outcomes: The outcome of this application is the production of aziridines, which are three-membered nitrogen-containing cyclic molecules. These molecules are important synthetic targets due to their substantial ring strain and resultant proclivity towards ring-opening reactions .
Application Summary: 2-Bromo-1-methoxynaphthalene can also be used to prepare biaryls or biheterocycles by palladium-catalyzed Ullmann coupling .
Methods of Application: The Ullmann coupling is a type of cross-coupling reaction, where 2-Bromo-1-methoxynaphthalene is reacted with another aryl compound in the presence of a palladium catalyst .
Results or Outcomes: The result of this application is the formation of biaryl or biheterocyclic compounds, which are commonly used in the synthesis of various organic compounds .
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