4-(5-(4-Bromophenyl)-3-(3-methoxyphenyl)-4,5-dihydro-1H-pyrazol-1-yl)benzenesulfonamide

98%

Reagent Code: #152762
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CAS Number 1222513-26-9

science Other reagents with same CAS 1222513-26-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 486.38 g/mol
Formula C₂₂H₂₀BrN₃O₃S
badge Registry Numbers
MDL Number MFCD28009507
inventory_2 Storage & Handling
Storage 2-8°C, dry

description Product Description

Used in pharmaceutical research as a key intermediate in the synthesis of anti-inflammatory and anticancer agents. Shows potential as a COX-2 inhibitor, contributing to the development of selective nonsteroidal anti-inflammatory drugs (NSAIDs). Also investigated for its role in modulating kinase pathways involved in tumor growth. Its sulfonamide and bromo-functionalized structure makes it valuable in structure-activity relationship (SAR) studies for optimizing drug candidates. Commonly employed in cross-coupling reactions to generate novel bioactive molecules.

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Size Availability Unit Price Quantity
inventory 5mg
10-20 days ฿8,050.00
inventory 50mg
10-20 days ฿46,410.00

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4-(5-(4-Bromophenyl)-3-(3-methoxyphenyl)-4,5-dihydro-1H-pyrazol-1-yl)benzenesulfonamide
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Used in pharmaceutical research as a key intermediate in the synthesis of anti-inflammatory and anticancer agents. Shows potential as a COX-2 inhibitor, contributing to the development of selective nonsteroidal anti-inflammatory drugs (NSAIDs). Also investigated for its role in modulating kinase pathways involved in tumor growth. Its sulfonamide and bromo-functionalized structure makes it valuable in structure-activity relationship (SAR) studies for optimizing drug candidates. Commonly employed in cross-

Used in pharmaceutical research as a key intermediate in the synthesis of anti-inflammatory and anticancer agents. Shows potential as a COX-2 inhibitor, contributing to the development of selective nonsteroidal anti-inflammatory drugs (NSAIDs). Also investigated for its role in modulating kinase pathways involved in tumor growth. Its sulfonamide and bromo-functionalized structure makes it valuable in structure-activity relationship (SAR) studies for optimizing drug candidates. Commonly employed in cross-coupling reactions to generate novel bioactive molecules.

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