5-Bromo-2-(methoxymethoxy)benzaldehyde

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Reagent Code: #154502
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CAS Number 68860-39-9

science Other reagents with same CAS 68860-39-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 245.07 g/mol
Formula C₉H₉BrO₃
badge Registry Numbers
MDL Number MFCD21195357
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of biologically active molecules. Its aldehyde and bromo functionalities allow for selective cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. The methoxymethoxy group acts as a protecting group for phenols, making it valuable in multi-step organic syntheses where chemoselectivity is required. Commonly employed in the preparation of heterocyclic compounds and natural product analogs with potential therapeutic properties.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿4,330.00
inventory 250mg
10-20 days ฿7,210.00
inventory 1g
10-20 days ฿15,140.00

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5-Bromo-2-(methoxymethoxy)benzaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of biologically active molecules. Its aldehyde and bromo functionalities allow for selective cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. The methoxymethoxy group acts as a protecting group for phenols, making it valuable in multi-step organic syntheses where chemoselectivity is required. Commonly employed in the preparatio

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of biologically active molecules. Its aldehyde and bromo functionalities allow for selective cross-coupling reactions, such as Suzuki or Heck reactions, enabling the construction of complex aromatic systems. The methoxymethoxy group acts as a protecting group for phenols, making it valuable in multi-step organic syntheses where chemoselectivity is required. Commonly employed in the preparation of heterocyclic compounds and natural product analogs with potential therapeutic properties.

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