N-(3-Carbamoyl-4,5,6,7-tetrahydro-benzo[b]thiophen-2-yl)-nicotinamide

98%

Reagent Code: #220235
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CAS Number 298207-49-5

science Other reagents with same CAS 298207-49-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 301.36 g/mol
Formula C₁₅H₁₅N₃O₂S
thermostat Physical Properties
Boiling Point 394.8±42.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.391±0.06 g/cm3(Predicted)
Storage -20°C

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of enzyme inhibitors. Shows potential in studies related to metabolic and neurological disorders due to its structural affinity with nicotinamide-based cofactors. Also employed in the design of small-molecule therapeutics targeting protein-protein interactions. Its amide-rich, heterocyclic framework enhances binding selectivity in medicinal chemistry applications.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿55,990.00
inventory 10mg
10-20 days ฿83,960.00

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N-(3-Carbamoyl-4,5,6,7-tetrahydro-benzo[b]thiophen-2-yl)-nicotinamide
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Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of enzyme inhibitors. Shows potential in studies related to metabolic and neurological disorders due to its structural affinity with nicotinamide-based cofactors. Also employed in the design of small-molecule therapeutics targeting protein-protein interactions. Its amide-rich, heterocyclic framework enhances binding selectivity in medicinal chemistry applications.

Used in pharmaceutical research as a key intermediate in the synthesis of biologically active compounds, particularly in the development of enzyme inhibitors. Shows potential in studies related to metabolic and neurological disorders due to its structural affinity with nicotinamide-based cofactors. Also employed in the design of small-molecule therapeutics targeting protein-protein interactions. Its amide-rich, heterocyclic framework enhances binding selectivity in medicinal chemistry applications.

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