5-(4-Fluorophenethylsulfonyl)-1-phenyl-1H-tetrazole

97%

Reagent Code: #187730
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CAS Number 1370411-43-0

science Other reagents with same CAS 1370411-43-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 332.35 g/mol
Formula C₁₅H₁₃FN₄O₂S
inventory_2 Storage & Handling
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of sulfonylurea derivatives, which exhibit potent herbicidal and fungicidal activities. It is employed in agrochemical research to develop new crop protection agents due to its ability to modulate enzyme activity in plants and fungi. The compound's structure allows for easy functionalization, making it valuable in medicinal chemistry for designing bioactive molecules. It has also been explored in the development of anti-inflammatory and antimicrobial agents owing to the tetrazole ring’s metabolic stability and resemblance to carboxylic acid bioisosteres. Its fluorinated aromatic group enhances membrane permeability and binding affinity in biological systems, useful in optimizing lead compounds during drug discovery.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 25mg
10-20 days ฿1,520.00
inventory 100mg
10-20 days ฿4,430.00
inventory 250mg
10-20 days ฿6,640.00
inventory 1g
10-20 days ฿16,600.00
5-(4-Fluorophenethylsulfonyl)-1-phenyl-1H-tetrazole
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Used as a key intermediate in the synthesis of sulfonylurea derivatives, which exhibit potent herbicidal and fungicidal activities. It is employed in agrochemical research to develop new crop protection agents due to its ability to modulate enzyme activity in plants and fungi. The compound's structure allows for easy functionalization, making it valuable in medicinal chemistry for designing bioactive molecules. It has also been explored in the development of anti-inflammatory and antimicrobial agents owing to the tetrazole ring’s metabolic stability and resemblance to carboxylic acid bioisosteres. Its fluorinated aromatic group enhances membrane permeability and binding affinity in biological systems, useful in optimizing lead compounds during drug discovery.
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