1-(4-(Trifluoromethyl)pyrimidin-2-yl)-1,4-diazepane

95%

Reagent Code: #238273
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CAS Number 238403-48-0

science Other reagents with same CAS 238403-48-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 246.23 g/mol
Formula C₁₀H₁₃F₃N₄
badge Registry Numbers
MDL Number MFCD00728997
thermostat Physical Properties
Melting Point 50 °C
Boiling Point 346.5±52.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.259±0.06 g/cm3(Predicted)
Storage 2-8°C, Inert Gas

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeting protein kinases involved in inflammatory diseases and cancer. Its structure allows for strong binding to enzyme active sites, enhancing selectivity and potency. Commonly employed in the development of small-molecule therapeutics due to its metabolic stability and ability to cross cell membranes. Also utilized in medicinal chemistry for optimizing lead compounds in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿8,990.00
inventory 5g
10-20 days ฿31,430.00
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1-(4-(Trifluoromethyl)pyrimidin-2-yl)-1,4-diazepane
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Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeting protein kinases involved in inflammatory diseases and cancer. Its structure allows for strong binding to enzyme active sites, enhancing selectivity and potency. Commonly employed in the development of small-molecule therapeutics due to its metabolic stability and ability to cross cell membranes. Also utilized in medicinal chemistry for optimizing lead compounds in drug discovery program

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly for targeting protein kinases involved in inflammatory diseases and cancer. Its structure allows for strong binding to enzyme active sites, enhancing selectivity and potency. Commonly employed in the development of small-molecule therapeutics due to its metabolic stability and ability to cross cell membranes. Also utilized in medicinal chemistry for optimizing lead compounds in drug discovery programs.

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