1-(4-Bromo-2-nitrophenyl)piperidine

95%

Reagent Code: #141253
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CAS Number 5465-66-7

science Other reagents with same CAS 5465-66-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 285.15 g/mol
Formula C₁₁H₁₃BrN₂O₂
badge Registry Numbers
MDL Number MFCD00087243
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used primarily as an intermediate in organic synthesis, this compound plays a key role in the development of pharmaceuticals and bioactive molecules. Its structure supports the construction of complex heterocyclic systems, often found in drug candidates targeting central nervous system disorders. The presence of both bromo and nitro functional groups allows for further transformations via cross-coupling reactions or reduction, enabling the introduction of diverse substituents. It is also employed in medicinal chemistry research for scaffold modification and structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,980.00
inventory 250mg
10-20 days ฿13,550.00
inventory 1g
10-20 days ฿36,590.00

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1-(4-Bromo-2-nitrophenyl)piperidine
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Used primarily as an intermediate in organic synthesis, this compound plays a key role in the development of pharmaceuticals and bioactive molecules. Its structure supports the construction of complex heterocyclic systems, often found in drug candidates targeting central nervous system disorders. The presence of both bromo and nitro functional groups allows for further transformations via cross-coupling reactions or reduction, enabling the introduction of diverse substituents. It is also employed in medi

Used primarily as an intermediate in organic synthesis, this compound plays a key role in the development of pharmaceuticals and bioactive molecules. Its structure supports the construction of complex heterocyclic systems, often found in drug candidates targeting central nervous system disorders. The presence of both bromo and nitro functional groups allows for further transformations via cross-coupling reactions or reduction, enabling the introduction of diverse substituents. It is also employed in medicinal chemistry research for scaffold modification and structure-activity relationship studies.

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