5,6,7,8-Tetrahydro-2-methyl-6-(phenylmethyl)pyrido[4,3-d]pyrimidin-4(3H)-one

95%

Reagent Code: #242742
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CAS Number 1448-40-4

science Other reagents with same CAS 1448-40-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 255.31 g/mol
Formula C₁₅H₁₇N₃O
badge Registry Numbers
MDL Number MFCD06776713
thermostat Physical Properties
Melting Point 195-197 °C
Boiling Point 412.6±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.24±0.1 g/cm3(Predicted)
Storage Room temperature

description Product Description

Used primarily in pharmaceutical research as an intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. It serves as a scaffold in the development of potential anticancer agents due to its ability to interact with specific enzyme targets involved in cell signaling pathways. Its structure allows for selective binding to ATP sites in kinases, making it valuable in designing drugs for targeted cancer therapies. Also investigated for use in central nervous system agents due to its ability to cross the blood-brain barrier.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days $94.07
inventory 250mg
10-20 days $181.16
inventory 1g
10-20 days $473.81

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5,6,7,8-Tetrahydro-2-methyl-6-(phenylmethyl)pyrido[4,3-d]pyrimidin-4(3H)-one
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Used primarily in pharmaceutical research as an intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. It serves as a scaffold in the development of potential anticancer agents due to its ability to interact with specific enzyme targets involved in cell signaling pathways. Its structure allows for selective binding to ATP sites in kinases, making it valuable in designing drugs for targeted cancer therapies. Also investigated for use in central nervous system agent

Used primarily in pharmaceutical research as an intermediate in the synthesis of biologically active compounds, particularly kinase inhibitors. It serves as a scaffold in the development of potential anticancer agents due to its ability to interact with specific enzyme targets involved in cell signaling pathways. Its structure allows for selective binding to ATP sites in kinases, making it valuable in designing drugs for targeted cancer therapies. Also investigated for use in central nervous system agents due to its ability to cross the blood-brain barrier.

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