3-(1-Phenylethyl)-2-thioxo-2,3-dihydroquinazolin-4(1H)-one

95%

Reagent Code: #223062
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CAS Number 568558-23-6

science Other reagents with same CAS 568558-23-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 282.36 g/mol
Formula C₁₆H₁₄N₂OS
badge Registry Numbers
MDL Number MFCD03985197
inventory_2 Storage & Handling
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals targeting central nervous system disorders. Exhibits potential as a scaffold in medicinal chemistry due to its affinity for benzodiazepine receptors, making it valuable in the design of anxiolytic and anticonvulsant agents. Also employed in research settings for structure-activity relationship studies of heterocyclic compounds. Its thioxo functionality enhances binding interactions in enzyme inhibition assays, particularly in kinase and protease inhibitor development.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿3,650.00
250mg
10-20 days ฿6,190.00
1g
10-20 days ฿16,710.00
3-(1-Phenylethyl)-2-thioxo-2,3-dihydroquinazolin-4(1H)-one
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Used as a key intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals targeting central nervous system disorders. Exhibits potential as a scaffold in medicinal chemistry due to its affinity for benzodiazepine receptors, making it valuable in the design of anxiolytic and anticonvulsant agents. Also employed in research settings for structure-activity relationship studies of heterocyclic compounds. Its thioxo functionality enhances binding interact

Used as a key intermediate in the synthesis of biologically active compounds, particularly in the development of pharmaceuticals targeting central nervous system disorders. Exhibits potential as a scaffold in medicinal chemistry due to its affinity for benzodiazepine receptors, making it valuable in the design of anxiolytic and anticonvulsant agents. Also employed in research settings for structure-activity relationship studies of heterocyclic compounds. Its thioxo functionality enhances binding interactions in enzyme inhibition assays, particularly in kinase and protease inhibitor development.

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