2-Bromo-1,3-dimethoxybenzene

98%

Reagent Code: #144308
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CAS Number 16932-45-9

science Other reagents with same CAS 16932-45-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 217.06 g/mol
Formula C₈H₉BrO₂
badge Registry Numbers
MDL Number MFCD07780177
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as an intermediate in organic synthesis, particularly in pharmaceuticals and agrochemicals. It serves as a building block for creating complex molecules through cross-coupling reactions like Suzuki or Heck reactions, where the bromine atom is readily displaced to form new carbon-carbon bonds. Its methoxy groups help direct electrophilic substitution and stabilize reaction intermediates. Commonly employed in the development of bioactive compounds, including drug candidates and functional materials.

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Test Parameter Specification
Purity (HPLC) 97.5-100
Melting Point (°C) 91-95
Appearance WHITE TO YELLOW TO BEIGE TO BROWN POWDER OR CRYSTALS

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿690.00
inventory 25g
10-20 days ฿2,500.00
inventory 100g
10-20 days ฿9,630.00
inventory 1g
10-20 days ฿180.00

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2-Bromo-1,3-dimethoxybenzene
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Used as an intermediate in organic synthesis, particularly in pharmaceuticals and agrochemicals. It serves as a building block for creating complex molecules through cross-coupling reactions like Suzuki or Heck reactions, where the bromine atom is readily displaced to form new carbon-carbon bonds. Its methoxy groups help direct electrophilic substitution and stabilize reaction intermediates. Commonly employed in the development of bioactive compounds, including drug candidates and functional materials.
Used as an intermediate in organic synthesis, particularly in pharmaceuticals and agrochemicals. It serves as a building block for creating complex molecules through cross-coupling reactions like Suzuki or Heck reactions, where the bromine atom is readily displaced to form new carbon-carbon bonds. Its methoxy groups help direct electrophilic substitution and stabilize reaction intermediates. Commonly employed in the development of bioactive compounds, including drug candidates and functional materials.
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