(E)-3-(2-(trifluoromethoxy)phenyl)acrylic acid

≥95%

Reagent Code: #181947
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CAS Number 399580-48-4

science Other reagents with same CAS 399580-48-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.16 g/mol
Formula C₁₀H₇F₃O₃
badge Registry Numbers
MDL Number MFCD06205273
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and antifungal agents. Its structure allows for conjugation into larger bioactive molecules, enhancing metabolic stability and binding affinity. Also employed in agrochemical formulations for crop protection due to its reactivity and ability to inhibit specific enzymes in pests. The trifluoromethoxy group contributes to improved lipophilicity and bioavailability in final active compounds.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,050.00
inventory 250mg
10-20 days ฿3,520.00
inventory 1g
10-20 days ฿10,590.00
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(E)-3-(2-(trifluoromethoxy)phenyl)acrylic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and antifungal agents. Its structure allows for conjugation into larger bioactive molecules, enhancing metabolic stability and binding affinity. Also employed in agrochemical formulations for crop protection due to its reactivity and ability to inhibit specific enzymes in pests. The trifluoromethoxy group contributes to improved lipophilicity and bioavailability in final active compounds.<

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and antifungal agents. Its structure allows for conjugation into larger bioactive molecules, enhancing metabolic stability and binding affinity. Also employed in agrochemical formulations for crop protection due to its reactivity and ability to inhibit specific enzymes in pests. The trifluoromethoxy group contributes to improved lipophilicity and bioavailability in final active compounds.

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