1-bromo-2-(methoxymethyl)benzene

98%

Reagent Code: #144121
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CAS Number 52711-30-5

science Other reagents with same CAS 52711-30-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 201.06 g/mol
Formula C₈H₉BrO
badge Registry Numbers
MDL Number MFCD03790887
thermostat Physical Properties
Boiling Point 213.0±15.0°C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, light-proof

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its bromine functionality allows for palladium-catalyzed cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. The methoxymethyl group serves as a protected hydroxymethyl functionality (equivalent to a methyl ether of a benzyl alcohol), which can be deprotected to the free benzyl alcohol using Lewis acids like BBr3. Commonly employed in the development of bioactive molecules where ortho-substituted benzene derivatives are required.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿950.00
inventory 1g
10-20 days ฿1,980.00
inventory 5g
10-20 days ฿6,540.00

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1-bromo-2-(methoxymethyl)benzene
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its bromine functionality allows for palladium-catalyzed cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. The methoxymethyl group serves as a protected hydroxymethyl functionality (equivalent to a methyl ether of a benzyl alcohol), which can be deprotected to the free benzyl alcohol using Lewis acids like BBr3. Commonly emplo

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its bromine functionality allows for palladium-catalyzed cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. The methoxymethyl group serves as a protected hydroxymethyl functionality (equivalent to a methyl ether of a benzyl alcohol), which can be deprotected to the free benzyl alcohol using Lewis acids like BBr3. Commonly employed in the development of bioactive molecules where ortho-substituted benzene derivatives are required.

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