N-[2-(4-bromophenoxy)ethyl]piperidinehydrochloride

98%

Reagent Code: #219614
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CAS Number 399016-75-2

science Other reagents with same CAS 399016-75-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 320.653 g/mol
Formula C₁₃H₁₉BrClNO
badge Registry Numbers
MDL Number MFCD08436985
thermostat Physical Properties
Boiling Point 392.5 °C at 760 mmHg
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) active agents. Its structure supports the creation of compounds with neuroreceptor affinity, making it valuable in research on serotonin and dopamine modulators. Commonly employed in medicinal chemistry for optimizing drug candidates targeting neurological disorders. Also utilized in the preparation of selective enzyme inhibitors due to its stable aromatic and amine functionality. Suitable for coupling reactions in heterocyclic compound design.

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inventory 500g
10-20 days ฿29,050.00

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N-[2-(4-bromophenoxy)ethyl]piperidinehydrochloride
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) active agents. Its structure supports the creation of compounds with neuroreceptor affinity, making it valuable in research on serotonin and dopamine modulators. Commonly employed in medicinal chemistry for optimizing drug candidates targeting neurological disorders. Also utilized in the preparation of selective enzyme inhibitors due to its stable aromatic and amine functionalit

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of central nervous system (CNS) active agents. Its structure supports the creation of compounds with neuroreceptor affinity, making it valuable in research on serotonin and dopamine modulators. Commonly employed in medicinal chemistry for optimizing drug candidates targeting neurological disorders. Also utilized in the preparation of selective enzyme inhibitors due to its stable aromatic and amine functionality. Suitable for coupling reactions in heterocyclic compound design.

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