(1-Pyrimidin-2-yl-piperidin-3-yl)-methanol

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Reagent Code: #227358
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CAS Number 419557-05-4

science Other reagents with same CAS 419557-05-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 193.246 g/mol
Formula C₁₀H₁₅N₃O
badge Registry Numbers
MDL Number MFCD01456244
inventory_2 Storage & Handling
Density 1.159 g/cm3
Storage Room temperature, seal, dry

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of central nervous system agents. Shows potential in the design of ligands targeting neurological receptors due to its structural compatibility with brain-targeted drugs. Also employed in the preparation of novel derivatives for screening antiviral and anti-inflammatory activities. Its hydroxyl and heterocyclic groups allow for easy functionalization, making it valuable in medicinal chemistry for structure-activity relationship studies.

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Size Availability Unit Price Quantity
inventory 500mg
10-20 days ฿18,540.00

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(1-Pyrimidin-2-yl-piperidin-3-yl)-methanol
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Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of central nervous system agents. Shows potential in the design of ligands targeting neurological receptors due to its structural compatibility with brain-targeted drugs. Also employed in the preparation of novel derivatives for screening antiviral and anti-inflammatory activities. Its hydroxyl and heterocyclic groups allow for easy functionalization, making it valuable

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of central nervous system agents. Shows potential in the design of ligands targeting neurological receptors due to its structural compatibility with brain-targeted drugs. Also employed in the preparation of novel derivatives for screening antiviral and anti-inflammatory activities. Its hydroxyl and heterocyclic groups allow for easy functionalization, making it valuable in medicinal chemistry for structure-activity relationship studies.

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