5-​Pyrimidinemethanamin​e, N-​[1-​(4-​chlorophenyl)​ethyl]​-​2-​(4-​morpholinyl)​-

95%

Reagent Code: #223390
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CAS Number 1280981-01-2

science Other reagents with same CAS 1280981-01-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 332.8278 g/mol
Formula C₁₇H₂₁ClN₄O
thermostat Physical Properties
Boiling Point 502.9±60.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.229±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used primarily as a pharmaceutical intermediate in the synthesis of bioactive compounds, particularly in the development of kinase inhibitors. It plays a role in the creation of molecules with potential antiviral and anticancer properties due to its ability to interact with specific enzyme targets. Its structure supports binding to ATP sites in kinases, making it valuable in drug discovery programs focused on signal transduction pathways. Also utilized in research settings to design novel therapeutic agents targeting inflammatory and proliferative diseases.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿14,400.00
inventory 100mg
10-20 days ฿40,000.00

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5-​Pyrimidinemethanamin​e, N-​[1-​(4-​chlorophenyl)​ethyl]​-​2-​(4-​morpholinyl)​-
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Used primarily as a pharmaceutical intermediate in the synthesis of bioactive compounds, particularly in the development of kinase inhibitors. It plays a role in the creation of molecules with potential antiviral and anticancer properties due to its ability to interact with specific enzyme targets. Its structure supports binding to ATP sites in kinases, making it valuable in drug discovery programs focused on signal transduction pathways. Also utilized in research settings to design novel therapeutic age

Used primarily as a pharmaceutical intermediate in the synthesis of bioactive compounds, particularly in the development of kinase inhibitors. It plays a role in the creation of molecules with potential antiviral and anticancer properties due to its ability to interact with specific enzyme targets. Its structure supports binding to ATP sites in kinases, making it valuable in drug discovery programs focused on signal transduction pathways. Also utilized in research settings to design novel therapeutic agents targeting inflammatory and proliferative diseases.

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