4-(Piperidin-1-yl)-1,2,5-thiadiazol-3-yl piperidine-1-carboxylate

97%

Reagent Code: #201709
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CAS Number 1234569-09-5

science Other reagents with same CAS 1234569-09-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 296.39 g/mol
Formula C₁₃H₂₀N₄O₂S
badge Registry Numbers
MDL Number MFCD31544494
thermostat Physical Properties
Boiling Point 438.5±45.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.295±0.06 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used as a key intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors for cancer treatment. Shows potential in medicinal chemistry for designing compounds with central nervous system activity due to its ability to cross the blood-brain barrier. Its structure supports high binding affinity to specific enzyme targets, making it valuable in creating selective therapeutic agents. Also employed in research for novel antiviral drugs owing to its heterocyclic stability and functional versatility.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿10,990.00
inventory 25mg
10-20 days ฿28,590.00
4-(Piperidin-1-yl)-1,2,5-thiadiazol-3-yl piperidine-1-carboxylate
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Used as a key intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors for cancer treatment. Shows potential in medicinal chemistry for designing compounds with central nervous system activity due to its ability to cross the blood-brain barrier. Its structure supports high binding affinity to specific enzyme targets, making it valuable in creating selective therapeutic agents. Also employed in research for novel antiviral drugs owing to its heterocyclic stability and

Used as a key intermediate in pharmaceutical synthesis, particularly in the development of kinase inhibitors for cancer treatment. Shows potential in medicinal chemistry for designing compounds with central nervous system activity due to its ability to cross the blood-brain barrier. Its structure supports high binding affinity to specific enzyme targets, making it valuable in creating selective therapeutic agents. Also employed in research for novel antiviral drugs owing to its heterocyclic stability and functional versatility.

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