4-(Benzyloxy)-2-bromophenol

95%

Reagent Code: #150790
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CAS Number 79352-66-2

science Other reagents with same CAS 79352-66-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 279.13 g/mol
Formula C₁₃H₁₁BrO₂
badge Registry Numbers
MDL Number MFCD03926352
thermostat Physical Properties
Melting Point 72-73 °C
Boiling Point 370.0±27.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.478±0.06 g/cm3(Predicted)
Storage Room temperature, light-proof storage, inert atmosphere

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of selective receptor modulators. It serves as a building block in the preparation of bioactive molecules due to the presence of both bromo and phenolic functional groups, which allow for further chemical modifications through cross-coupling reactions and ether formation. Its benzyl-protected phenol group enables controlled deprotection under mild conditions, making it valuable in multi-step organic syntheses. Also employed in the production of specialty polymers and ligands for catalysis.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,750.00
inventory 250mg
10-20 days ฿4,310.00
inventory 500mg
10-20 days ฿8,310.00
inventory 1g
10-20 days ฿16,000.00
4-(Benzyloxy)-2-bromophenol
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of selective receptor modulators. It serves as a building block in the preparation of bioactive molecules due to the presence of both bromo and phenolic functional groups, which allow for further chemical modifications through cross-coupling reactions and ether formation. Its benzyl-protected phenol group enables controlled deprotection under mild conditions, making it valuable in multi-step org

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of selective receptor modulators. It serves as a building block in the preparation of bioactive molecules due to the presence of both bromo and phenolic functional groups, which allow for further chemical modifications through cross-coupling reactions and ether formation. Its benzyl-protected phenol group enables controlled deprotection under mild conditions, making it valuable in multi-step organic syntheses. Also employed in the production of specialty polymers and ligands for catalysis.

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