4-(benzyloxy)-1-bromo-2-nitrobenzene

95%

Reagent Code: #150448
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CAS Number 4514-28-7

science Other reagents with same CAS 4514-28-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 308.13 g/mol
Formula C₁₃H₁₀BrNO₃
badge Registry Numbers
MDL Number MFCD28098598
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its functional groups—bromine, nitro, and benzyloxy—allow for selective transformations such as cross-coupling reactions, nucleophilic substitutions, and reductions. The bromo group is suitable for palladium-catalyzed coupling reactions like Suzuki or Heck reactions, enabling the construction of complex aromatic systems. The nitro group can be reduced to an amine, which serves as a precursor for diazotization or amide formation. The benzyloxy moiety acts as a protecting group for phenols and can be removed under mild conditions, making this compound valuable in multi-step synthesis where controlled deprotection is required.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿990.00
inventory 250mg
10-20 days ฿1,850.00
inventory 1g
10-20 days ฿3,710.00

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4-(benzyloxy)-1-bromo-2-nitrobenzene
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Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its functional groups—bromine, nitro, and benzyloxy—allow for selective transformations such as cross-coupling reactions, nucleophilic substitutions, and reductions. The bromo group is suitable for palladium-catalyzed coupling reactions like Suzuki or Heck reactions, enabling the construction of complex aromatic systems. The nitro group can be reduced to an amine, which serves as a precurso

Used as an intermediate in organic synthesis, particularly in the preparation of pharmaceuticals and agrochemicals. Its functional groups—bromine, nitro, and benzyloxy—allow for selective transformations such as cross-coupling reactions, nucleophilic substitutions, and reductions. The bromo group is suitable for palladium-catalyzed coupling reactions like Suzuki or Heck reactions, enabling the construction of complex aromatic systems. The nitro group can be reduced to an amine, which serves as a precursor for diazotization or amide formation. The benzyloxy moiety acts as a protecting group for phenols and can be removed under mild conditions, making this compound valuable in multi-step synthesis where controlled deprotection is required.

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