6-methyl-3-(prop-2-en-1-yl)-2-sulfanyl-5,6,7,8-tetrahydro[1]benzothieno[2,3-d]pyrimidin-4(3H)-one

98%

Reagent Code: #245702
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CAS Number 331964-66-0

science Other reagents with same CAS 331964-66-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 292.42 g/mol
Formula C₁₄H₁₆N₂OS₂
thermostat Physical Properties
Boiling Point 467.4±55.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.34±0.1 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors. Shows potential in studies related to anti-inflammatory and anticancer agents due to its ability to interact with specific enzyme targets. Also employed in the design of novel heterocyclic systems for drug discovery, where its fused ring structure enhances binding affinity and selectivity.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿28,590.00
inventory 5mg
10-20 days ฿8,790.00

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6-methyl-3-(prop-2-en-1-yl)-2-sulfanyl-5,6,7,8-tetrahydro[1]benzothieno[2,3-d]pyrimidin-4(3H)-one
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Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors. Shows potential in studies related to anti-inflammatory and anticancer agents due to its ability to interact with specific enzyme targets. Also employed in the design of novel heterocyclic systems for drug discovery, where its fused ring structure enhances binding affinity and selectivity.
Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of kinase inhibitors. Shows potential in studies related to anti-inflammatory and anticancer agents due to its ability to interact with specific enzyme targets. Also employed in the design of novel heterocyclic systems for drug discovery, where its fused ring structure enhances binding affinity and selectivity.
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