2-Bromo-6-methoxy-3,4-dihydronaphthalen-1(2H)-one

95%

  • Product Code: 82385
  CAS:    20933-24-8
Molecular Weight: 255.11 g./mol Molecular Formula: C₁₁H₁₁BrO₂
EC Number: MDL Number: MFCD09056778
Melting Point: 78-79 °C Boiling Point: 367.642° °C(Predicted)
Density: 1.490±0.06 g/cm3(Predicted) Storage Condition: 2-8°C, sealed, dry
Product Description: This compound is primarily utilized in organic synthesis as an intermediate in the production of more complex molecules. Its structure, featuring both bromine and methoxy groups, makes it a versatile building block in the development of pharmaceuticals, particularly in the synthesis of compounds with potential therapeutic properties. It is often employed in cross-coupling reactions, where the bromine atom facilitates the formation of carbon-carbon bonds, essential for constructing intricate organic frameworks. Additionally, its dihydronaphthalenone core is valuable in the creation of compounds with applications in materials science, such as organic semiconductors or light-emitting materials. Researchers also explore its use in the synthesis of natural product analogs, leveraging its reactivity to mimic or modify biologically active structures.
Sizes / Availability / Pricing:
Size (g) Availability Price Quantity
0.100 10-20 days ฿4,860.00
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0.250 10-20 days ฿9,495.00
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1.000 10-20 days ฿18,900.00
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2-Bromo-6-methoxy-3,4-dihydronaphthalen-1(2H)-one
This compound is primarily utilized in organic synthesis as an intermediate in the production of more complex molecules. Its structure, featuring both bromine and methoxy groups, makes it a versatile building block in the development of pharmaceuticals, particularly in the synthesis of compounds with potential therapeutic properties. It is often employed in cross-coupling reactions, where the bromine atom facilitates the formation of carbon-carbon bonds, essential for constructing intricate organic frameworks. Additionally, its dihydronaphthalenone core is valuable in the creation of compounds with applications in materials science, such as organic semiconductors or light-emitting materials. Researchers also explore its use in the synthesis of natural product analogs, leveraging its reactivity to mimic or modify biologically active structures.
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