N-(3-chloro-4-hydroxyphenyl)-2-oxo-1,2-dihydrobenzo[cd]indole-6-sulfonamide

98%

Reagent Code: #245670
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CAS Number 397281-20-8

science Other reagents with same CAS 397281-20-8

blur_circular Chemical Specifications

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Weight 374.8 g/mol
Formula C₁₇H₁₁ClN₂O₄S
inventory_2 Storage & Handling
Density 1.651±0.06 g/cm3(Predicted)
Storage Room temperature, seal, dry

description Product Description

Used as a key intermediate in the synthesis of indole-based pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its sulfonamide and hydroxyl functional groups enable strong binding to biological targets, enhancing selectivity and potency. Also employed in research for designing anti-inflammatory and antiproliferative agents due to its ability to modulate cellular signaling pathways. The compound’s structure supports derivatization for optimizing drug-like properties in medicinal chemistry programs.

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Size Availability Unit Price Quantity
inventory 1mg
10-20 days ฿1,980.00
inventory 5mg
10-20 days ฿7,920.00

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N-(3-chloro-4-hydroxyphenyl)-2-oxo-1,2-dihydrobenzo[cd]indole-6-sulfonamide
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Used as a key intermediate in the synthesis of indole-based pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its sulfonamide and hydroxyl functional groups enable strong binding to biological targets, enhancing selectivity and potency. Also employed in research for designing anti-inflammatory and antiproliferative agents due to its ability to modulate cellular signaling pathways. The compound’s structure supports derivatization for optimizing drug-like propertie

Used as a key intermediate in the synthesis of indole-based pharmaceuticals, particularly in the development of kinase inhibitors for cancer treatment. Its sulfonamide and hydroxyl functional groups enable strong binding to biological targets, enhancing selectivity and potency. Also employed in research for designing anti-inflammatory and antiproliferative agents due to its ability to modulate cellular signaling pathways. The compound’s structure supports derivatization for optimizing drug-like properties in medicinal chemistry programs.

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