Ethyl 2-(3-benzoylthioureido)-5,5-dimethyl-4,7-dihydro-5H-thieno[2,3-c]pyran-3-carboxylate

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Reagent Code: #185250
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CAS Number 314042-00-7

science Other reagents with same CAS 314042-00-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 418.53 g/mol
Formula C₂₀H₂₂N₂O₄S₂
inventory_2 Storage & Handling
Storage 2-8°C, drying away from light

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active heterocyclic compounds. Shows potential in the development of anti-inflammatory and antimicrobial agents due to its structural features involving thioureido and fused thienopyran moieties. Also employed in studies focused on enzyme inhibition, particularly in models targeting oxidative stress-related pathways. Its ester functionality allows for easy modification, making it valuable in structure-activity relationship (SAR) studies during drug design.

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Size Availability Unit Price Quantity
inventory 50mg
10-20 days ฿5,700.00
inventory 100mg
10-20 days ฿6,390.00
inventory 250mg
10-20 days ฿12,900.00
inventory 1g
10-20 days ฿36,030.00

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Ethyl 2-(3-benzoylthioureido)-5,5-dimethyl-4,7-dihydro-5H-thieno[2,3-c]pyran-3-carboxylate
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Used in pharmaceutical research as a key intermediate in the synthesis of biologically active heterocyclic compounds. Shows potential in the development of anti-inflammatory and antimicrobial agents due to its structural features involving thioureido and fused thienopyran moieties. Also employed in studies focused on enzyme inhibition, particularly in models targeting oxidative stress-related pathways. Its ester functionality allows for easy modification, making it valuable in structure-activity relation

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active heterocyclic compounds. Shows potential in the development of anti-inflammatory and antimicrobial agents due to its structural features involving thioureido and fused thienopyran moieties. Also employed in studies focused on enzyme inhibition, particularly in models targeting oxidative stress-related pathways. Its ester functionality allows for easy modification, making it valuable in structure-activity relationship (SAR) studies during drug design.

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