2,2-Difluorobenzo[d][1,3]dioxol-5-ol

98%

Reagent Code: #177849
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CAS Number 1211539-82-0

science Other reagents with same CAS 1211539-82-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 174.104 g/mol
Formula C₇H₄F₂O₃
badge Registry Numbers
MDL Number MFCD22414499
thermostat Physical Properties
Boiling Point 212.9 °C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, inert gas

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to its unique difluoromethylene-dioxole structure. Its electron-withdrawing fluorine atoms enhance metabolic stability and bioavailability in drug candidates. Commonly employed in the development of bioactive molecules, particularly in medicinal chemistry for designing enzyme inhibitors and receptor modulators. Also utilized in the preparation of novel fluorinated building blocks for PET tracer development, where fluorine-18 labeling benefits from the presence of fluorine atoms in close proximity. Shows utility in materials science for creating specialty polymers with improved thermal and oxidative resistance.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿7,350.00
inventory 250mg
10-20 days ฿9,550.00
inventory 1g
10-20 days ฿28,560.00
inventory 5g
10-20 days ฿71,880.00

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2,2-Difluorobenzo[d][1,3]dioxol-5-ol
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Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to its unique difluoromethylene-dioxole structure. Its electron-withdrawing fluorine atoms enhance metabolic stability and bioavailability in drug candidates. Commonly employed in the development of bioactive molecules, particularly in medicinal chemistry for designing enzyme inhibitors and receptor modulators. Also utilized in the preparation of novel fluorinated building blocks for PET tracer development, w

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals and agrochemicals due to its unique difluoromethylene-dioxole structure. Its electron-withdrawing fluorine atoms enhance metabolic stability and bioavailability in drug candidates. Commonly employed in the development of bioactive molecules, particularly in medicinal chemistry for designing enzyme inhibitors and receptor modulators. Also utilized in the preparation of novel fluorinated building blocks for PET tracer development, where fluorine-18 labeling benefits from the presence of fluorine atoms in close proximity. Shows utility in materials science for creating specialty polymers with improved thermal and oxidative resistance.

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