N-(4-methylthiazol-2-yl)-5,6-dihydro-4H-cyclopenta[b]thiophene-2-carboxamide

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Reagent Code: #245675
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CAS Number 380471-64-7

science Other reagents with same CAS 380471-64-7

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Weight 264.37 g/mol
Formula C₁₂H₁₂N₂OS₂
inventory_2 Storage & Handling
Density 1.422±0.06 g/cm3(Predicted)
Storage -20°C, Sealed, Dry

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly targeting enzymes involved in inflammatory and oncogenic pathways. Shows potential in the development of anti-cancer agents due to its ability to modulate cell signaling proteins. Also explored for use in dermatological treatments owing to its stability and permeability across biological membranes. Employed in structure-activity relationship (SAR) studies to optimize potency and selectivity in drug candidates.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿4,390.00
inventory 25mg
10-20 days ฿13,190.00

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N-(4-methylthiazol-2-yl)-5,6-dihydro-4H-cyclopenta[b]thiophene-2-carboxamide
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Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly targeting enzymes involved in inflammatory and oncogenic pathways. Shows potential in the development of anti-cancer agents due to its ability to modulate cell signaling proteins. Also explored for use in dermatological treatments owing to its stability and permeability across biological membranes. Employed in structure-activity relationship (SAR) studies to optimize potency and selectivity in drug c

Used in pharmaceutical research as a key intermediate in the synthesis of kinase inhibitors, particularly targeting enzymes involved in inflammatory and oncogenic pathways. Shows potential in the development of anti-cancer agents due to its ability to modulate cell signaling proteins. Also explored for use in dermatological treatments owing to its stability and permeability across biological membranes. Employed in structure-activity relationship (SAR) studies to optimize potency and selectivity in drug candidates.

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