4-(Difluoromethoxy)-3-hydroxybenzoic acid

96%

Reagent Code: #177299
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CAS Number 913985-07-6

science Other reagents with same CAS 913985-07-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 204.13 g/mol
Formula C₈H₆F₂O₄
badge Registry Numbers
MDL Number MFCD24497448
inventory_2 Storage & Handling
Storage 2-8°C, inert gas storage

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of anti-inflammatory and antimicrobial agents. Its structure supports enhanced metabolic stability and bioavailability in drug candidates. Commonly employed in research for designing enzyme inhibitors due to the combined effect of the hydroxyl and difluoromethoxy groups, which improve binding affinity to target proteins. Also utilized in agrochemical research for developing herbicides and fungicides with improved environmental persistence and activity under varied pH conditions.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿1,010.00
inventory 250mg
10-20 days ฿2,330.00

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4-(Difluoromethoxy)-3-hydroxybenzoic acid
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Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of anti-inflammatory and antimicrobial agents. Its structure supports enhanced metabolic stability and bioavailability in drug candidates. Commonly employed in research for designing enzyme inhibitors due to the combined effect of the hydroxyl and difluoromethoxy groups, which improve binding affinity to target proteins. Also utilized in agrochemical research for developing herbicides and fungicide

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of anti-inflammatory and antimicrobial agents. Its structure supports enhanced metabolic stability and bioavailability in drug candidates. Commonly employed in research for designing enzyme inhibitors due to the combined effect of the hydroxyl and difluoromethoxy groups, which improve binding affinity to target proteins. Also utilized in agrochemical research for developing herbicides and fungicides with improved environmental persistence and activity under varied pH conditions.

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