4-Bromo-5-chloro-N-(2,4-dimethoxybenzyl)-2-fluoro-N-(thiazol-2-yl)benzenesulfonamide

97%

Reagent Code: #155575
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CAS Number 2342604-44-6

science Other reagents with same CAS 2342604-44-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 521.81 g/mol
Formula C₁₈H₁₅BrClFN₂O₄S₂
badge Registry Numbers
MDL Number MFCD31630952
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of sulfonamide-based bioactive compounds. Its structural features enable it to act as a building block for novel sulfonamide derivatives with potential antimicrobial and antifungal properties. The presence of halogen atoms and the thiazole ring facilitates cross-coupling reactions, making it valuable in medicinal chemistry for structure-activity relationship studies. It is also employed in the preparation of enzyme inhibitors targeting specific metabolic pathways in pathogenic organisms.

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inventory 100mg
10-20 days ฿30,850.00

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4-Bromo-5-chloro-N-(2,4-dimethoxybenzyl)-2-fluoro-N-(thiazol-2-yl)benzenesulfonamide
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Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of sulfonamide-based bioactive compounds. Its structural features enable it to act as a building block for novel sulfonamide derivatives with potential antimicrobial and antifungal properties. The presence of halogen atoms and the thiazole ring facilitates cross-coupling reactions, making it valuable in medicinal chemistry for structure-activity relationship studies. It is also employed in th

Used as a key intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of sulfonamide-based bioactive compounds. Its structural features enable it to act as a building block for novel sulfonamide derivatives with potential antimicrobial and antifungal properties. The presence of halogen atoms and the thiazole ring facilitates cross-coupling reactions, making it valuable in medicinal chemistry for structure-activity relationship studies. It is also employed in the preparation of enzyme inhibitors targeting specific metabolic pathways in pathogenic organisms.

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