2-Bromo-6-methoxynaphthalene

98%

Reagent Code: #144435
label
Alias 6-Methoxy-2-Bromonaphthalene
fingerprint
CAS Number 5111-65-9

science Other reagents with same CAS 5111-65-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 237.10 g/mol
Formula C₁₁H₉BrO
badge Registry Numbers
MDL Number MFCD00004062
inventory_2 Storage & Handling
Storage Room temperature, sealed

description Product Description

Used primarily as an intermediate in the synthesis of pharmaceuticals, especially nonsteroidal anti-inflammatory drugs (NSAIDs) like naproxen. Its structure allows for selective functionalization, making it valuable in creating chiral molecules through asymmetric synthesis. Also employed in the production of agrochemicals and specialty organic compounds where naphthalene derivatives are required. Its bromo and methoxy groups serve as reactive sites for coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems in medicinal chemistry and materials science.

format_list_bulleted Product Specification

Test Parameter Specification
Appearance White to Off-White to Light brown Powder
Purity (%) 97.5-100%
Infrared Spectrum Conforms to Structure
Melting Point (°C) 107-111

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿320.00
inventory 25g
10-20 days ฿1,020.00
inventory 100g
10-20 days ฿4,000.00
inventory 500g
10-20 days ฿16,460.00
inventory 2.5kg
10-20 days ฿80,560.00

Cart

No products

Subtotal: 0.00
Total 0.00 THB
2-Bromo-6-methoxynaphthalene
No image available

Used primarily as an intermediate in the synthesis of pharmaceuticals, especially nonsteroidal anti-inflammatory drugs (NSAIDs) like naproxen. Its structure allows for selective functionalization, making it valuable in creating chiral molecules through asymmetric synthesis. Also employed in the production of agrochemicals and specialty organic compounds where naphthalene derivatives are required. Its bromo and methoxy groups serve as reactive sites for coupling reactions, such as Suzuki or Heck reactions

Used primarily as an intermediate in the synthesis of pharmaceuticals, especially nonsteroidal anti-inflammatory drugs (NSAIDs) like naproxen. Its structure allows for selective functionalization, making it valuable in creating chiral molecules through asymmetric synthesis. Also employed in the production of agrochemicals and specialty organic compounds where naphthalene derivatives are required. Its bromo and methoxy groups serve as reactive sites for coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems in medicinal chemistry and materials science.

Mechanism -
Appearance -
Longevity -
Strength -
Storage -
Shelf Life -
Allergen(s) -
Dosage (Range) -
Dosage (Per Day) -
Mix Method -
Heat Resistance -
Stable in pH range -
Solubility -
Product Types -
INCI -

Purchase History for

Loading purchase history...