N-(4-Fluorophenyl)-N-isopropyl-2-((5-(trifluoromethyl)-1,3,4-thiadiazol-2-yl)oxy)acetamide

95%

Reagent Code: #215360
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Alias Fluthiamin
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CAS Number 142459-58-3

science Other reagents with same CAS 142459-58-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 363.33 g/mol
Formula C₁₄H₁₃F₄N₃O₂S
badge Registry Numbers
MDL Number MFCD01751191
thermostat Physical Properties
Melting Point 75-77 °C (lit.)
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and antimicrobial compounds. Its structure supports enhanced metabolic stability and bioavailability, making it valuable in optimizing drug candidates targeting central nervous system disorders and infectious diseases. Commonly employed in medicinal chemistry research for structure-activity relationship (SAR) studies due to the electron-withdrawing trifluoromethyl and fluorophenyl groups that influence binding affinity and selectivity. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and environmental safety profiles.

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Size Availability Unit Price Quantity
inventory 25g
10-20 days ฿1,400.00
inventory 100g
10-20 days ฿5,340.00

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N-(4-Fluorophenyl)-N-isopropyl-2-((5-(trifluoromethyl)-1,3,4-thiadiazol-2-yl)oxy)acetamide
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Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and antimicrobial compounds. Its structure supports enhanced metabolic stability and bioavailability, making it valuable in optimizing drug candidates targeting central nervous system disorders and infectious diseases. Commonly employed in medicinal chemistry research for structure-activity relationship (SAR) studies due to the electron-withdrawing trifluoromethyl and fluorophenyl gr

Used as a key intermediate in the synthesis of pharmaceutical agents, particularly in the development of anti-inflammatory and antimicrobial compounds. Its structure supports enhanced metabolic stability and bioavailability, making it valuable in optimizing drug candidates targeting central nervous system disorders and infectious diseases. Commonly employed in medicinal chemistry research for structure-activity relationship (SAR) studies due to the electron-withdrawing trifluoromethyl and fluorophenyl groups that influence binding affinity and selectivity. Also utilized in agrochemical research for designing novel pesticides with improved efficacy and environmental safety profiles.

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