2-(4-Chlorophenyl)-N-(2-methoxy-5-(piperidin-1-ylsulfonyl)phenyl)acetamide

98%

Reagent Code: #215809
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CAS Number 940850-10-2

science Other reagents with same CAS 940850-10-2

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Weight 422.93 g/mol
Formula C₂₀H₂₃ClN₂O₄S
inventory_2 Storage & Handling
Density 1.344±0.06 g/cm3(Predicted)
Storage 2-8°C, sealed, dry

description Product Description

Used in pharmaceutical research as a key intermediate for developing bioactive molecules, particularly in the synthesis of kinase inhibitors. Shows potential in anti-inflammatory and anticancer applications due to its ability to modulate specific cellular signaling pathways. Also employed in the design of selective receptor antagonists, making it valuable in neuropharmacology studies. Its sulfonamide and chlorophenyl groups enhance binding affinity to target proteins, improving drug efficacy in preclinical models.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿30,500.00
inventory 250mg
10-20 days ฿51,850.00

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2-(4-Chlorophenyl)-N-(2-methoxy-5-(piperidin-1-ylsulfonyl)phenyl)acetamide
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Used in pharmaceutical research as a key intermediate for developing bioactive molecules, particularly in the synthesis of kinase inhibitors. Shows potential in anti-inflammatory and anticancer applications due to its ability to modulate specific cellular signaling pathways. Also employed in the design of selective receptor antagonists, making it valuable in neuropharmacology studies. Its sulfonamide and chlorophenyl groups enhance binding affinity to target proteins, improving drug efficacy in preclinic

Used in pharmaceutical research as a key intermediate for developing bioactive molecules, particularly in the synthesis of kinase inhibitors. Shows potential in anti-inflammatory and anticancer applications due to its ability to modulate specific cellular signaling pathways. Also employed in the design of selective receptor antagonists, making it valuable in neuropharmacology studies. Its sulfonamide and chlorophenyl groups enhance binding affinity to target proteins, improving drug efficacy in preclinical models.

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