1-(Pyridin-3-yl)-1,4-diazepane

97%

Reagent Code: #226268
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CAS Number 223796-20-1

science Other reagents with same CAS 223796-20-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.25 g/mol
Formula C₁₀H₁₅N₃
badge Registry Numbers
MDL Number MFCD06409205
thermostat Physical Properties
Boiling Point 324.5°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, protected from light, stored in inert gas

description Product Description

Used in pharmaceutical research as a key scaffold for developing central nervous system (CNS) agents. Shows potential in the design of ligands targeting serotonin and dopamine receptors, particularly for treating neurological disorders such as depression, schizophrenia, and Parkinson’s disease. Its structure allows for good blood-brain barrier penetration, making it suitable for neuroactive drug development. Also employed in the synthesis of novel kinase inhibitors for oncology applications. Commonly modified to improve selectivity, metabolic stability, and bioavailability in drug candidates.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿9,180.00
inventory 250mg
10-20 days ฿18,340.00

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1-(Pyridin-3-yl)-1,4-diazepane
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Used in pharmaceutical research as a key scaffold for developing central nervous system (CNS) agents. Shows potential in the design of ligands targeting serotonin and dopamine receptors, particularly for treating neurological disorders such as depression, schizophrenia, and Parkinson’s disease. Its structure allows for good blood-brain barrier penetration, making it suitable for neuroactive drug development. Also employed in the synthesis of novel kinase inhibitors for oncology applications. Commonly mod

Used in pharmaceutical research as a key scaffold for developing central nervous system (CNS) agents. Shows potential in the design of ligands targeting serotonin and dopamine receptors, particularly for treating neurological disorders such as depression, schizophrenia, and Parkinson’s disease. Its structure allows for good blood-brain barrier penetration, making it suitable for neuroactive drug development. Also employed in the synthesis of novel kinase inhibitors for oncology applications. Commonly modified to improve selectivity, metabolic stability, and bioavailability in drug candidates.

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