2-(Methylthio)-5,6,7,8-tetrahydroquinazolin-4(3H)-one

97%

Reagent Code: #207137
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CAS Number 34170-21-3

science Other reagents with same CAS 34170-21-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 196.27 g/mol
Formula C₉H₁₂N₂OS
badge Registry Numbers
MDL Number MFCD08744204
thermostat Physical Properties
Melting Point 220-222°C
inventory_2 Storage & Handling
Storage 2-8°C

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 central nervous system disorders due to its structural affinity with neurotransmitter modulators. Also employed in agrochemical research for designing novel pesticides with improved selectivity. Its sulfur-containing scaffold enhances binding properties in enzyme inhibition assays, making it valuable in medicinal chemistry for optimizing lead compounds.

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Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿620.00
inventory 100mg
10-20 days ฿1,180.00

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2-(Methylthio)-5,6,7,8-tetrahydroquinazolin-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 central nervous system disorders due to its structural affinity with neurotransmitter modulators. Also employed in agrochemical research for designing novel pesticides with improved selectivity. Its sulfur-containing scaffold enhances binding properties in enzyme inhibition assays, making it valuable in medicin

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 central nervous system disorders due to its structural affinity with neurotransmitter modulators. Also employed in agrochemical research for designing novel pesticides with improved selectivity. Its sulfur-containing scaffold enhances binding properties in enzyme inhibition assays, making it valuable in medicinal chemistry for optimizing lead compounds.

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