2-Bromo-3-methoxynaphthalene

97%

Reagent Code: #147497
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CAS Number 68251-77-4

science Other reagents with same CAS 68251-77-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.1 g/mol
Formula C₁₁H₉BrO
thermostat Physical Properties
Melting Point 75°C
inventory_2 Storage & Handling
Storage Room temperature, stored in inert gas

description Product Description

Used as an intermediate in the synthesis of dyes and fluorescent compounds due to its aromatic structure and reactive bromine site. The presence of the methoxy group enhances electron density, making it suitable for coupling reactions in organic electronics and pharmaceuticals. Commonly employed in the preparation of naphthalene-based derivatives for use in agrochemicals and bioactive molecules. Its bromine functionality allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions.

Available Sizes & Pricing

Size Availability Unit Price Quantity
200mg
10-20 days ฿148.50
1g
10-20 days ฿380.00
5g
10-20 days ฿1,340.00
25g
10-20 days ฿6,470.00
100g
10-20 days ฿24,610.00
2-Bromo-3-methoxynaphthalene
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Used as an intermediate in the synthesis of dyes and fluorescent compounds due to its aromatic structure and reactive bromine site. The presence of the methoxy group enhances electron density, making it suitable for coupling reactions in organic electronics and pharmaceuticals. Commonly employed in the preparation of naphthalene-based derivatives for use in agrochemicals and bioactive molecules. Its bromine functionality allows for further functionalization via cross-coupling reactions such as Suzuki or

Used as an intermediate in the synthesis of dyes and fluorescent compounds due to its aromatic structure and reactive bromine site. The presence of the methoxy group enhances electron density, making it suitable for coupling reactions in organic electronics and pharmaceuticals. Commonly employed in the preparation of naphthalene-based derivatives for use in agrochemicals and bioactive molecules. Its bromine functionality allows for further functionalization via cross-coupling reactions such as Suzuki or Heck reactions.

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