4-Amino-3-(trifluoromethoxy)benzoic acid

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Reagent Code: #134912
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CAS Number 175278-22-5

science Other reagents with same CAS 175278-22-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.14 g/mol
Formula C₈H₆F₃NO₃
badge Registry Numbers
MDL Number MFCD00205143
thermostat Physical Properties
Melting Point 168 °C
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 analgesic agents. Its structure supports the creation of compounds with enhanced metabolic stability due to the presence of the trifluoromethoxy group. Commonly employed in the preparation of selective COX-2 inhibitors and other bioactive molecules where fluorinated aromatic rings improve potency and pharmacokinetic properties. Also utilized in agrochemical research for designing novel herbicides and pesticides with improved environmental stability.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿885.50
inventory 25g
10-20 days ฿4,158.00

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4-Amino-3-(trifluoromethoxy)benzoic acid
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. Its structure supports the creation of compounds with enhanced metabolic stability due to the presence of the trifluoromethoxy group. Commonly employed in the preparation of selective COX-2 inhibitors and other bioactive molecules where fluorinated aromatic rings improve potency and pharmacokinetic properties. Also utilized in agrochemical research for designing novel

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of anti-inflammatory and analgesic agents. Its structure supports the creation of compounds with enhanced metabolic stability due to the presence of the trifluoromethoxy group. Commonly employed in the preparation of selective COX-2 inhibitors and other bioactive molecules where fluorinated aromatic rings improve potency and pharmacokinetic properties. Also utilized in agrochemical research for designing novel herbicides and pesticides with improved environmental stability.

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