3-(Difluoromethoxy)-4-hydroxybenzaldehyde

95%

Reagent Code: #171090
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CAS Number 53173-70-9

science Other reagents with same CAS 53173-70-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 188.13 g/mol
Formula C₈H₆F₂O₃
thermostat Physical Properties
Melting Point 76-77°C
Boiling Point 276.2±35.0°C
inventory_2 Storage & Handling
Storage 2-8°C, inert gas atmosphere

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of proton pump inhibitors (PPIs) for treating gastric acid-related disorders. Its structure supports the formation of active compounds that inhibit the H+/K+-ATPase enzyme in the stomach lining. Commonly employed in the production of drugs like ilaprazole and other benzimidazole derivatives. Also utilized in research for developing new anti-ulcer agents due to its favorable reactivity and functional group arrangement.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,880.00
inventory 250mg
10-20 days ฿12,800.00
inventory 500mg
10-20 days ฿23,040.00

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3-(Difluoromethoxy)-4-hydroxybenzaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of proton pump inhibitors (PPIs) for treating gastric acid-related disorders. Its structure supports the formation of active compounds that inhibit the H+/K+-ATPase enzyme in the stomach lining. Commonly employed in the production of drugs like ilaprazole and other benzimidazole derivatives. Also utilized in research for developing new anti-ulcer agents due to its favorable reactivity and functional group arra

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the development of proton pump inhibitors (PPIs) for treating gastric acid-related disorders. Its structure supports the formation of active compounds that inhibit the H+/K+-ATPase enzyme in the stomach lining. Commonly employed in the production of drugs like ilaprazole and other benzimidazole derivatives. Also utilized in research for developing new anti-ulcer agents due to its favorable reactivity and functional group arrangement.

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