1-(2,4-Difluorophenyl)ethanol

95%

Reagent Code: #177226
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CAS Number 2267-47-2

science Other reagents with same CAS 2267-47-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 158.15 g/mol
Formula C₈H₈F₂O
badge Registry Numbers
MDL Number MFCD08442352
thermostat Physical Properties
Boiling Point 91-91.5 °C(Press: 15 Torr)
inventory_2 Storage & Handling
Density 1.226±0.06 g/cm3(Predicted)
Storage 2-8°C

description Product Description

Used as a key intermediate in the synthesis of antifungal agents, particularly in the production of fluconazole and related triazole antifungals. Its structure supports the formation of bioactive molecules that inhibit fungal cytochrome P450 enzymes, essential for ergosterol biosynthesis. Also utilized in the development of pharmaceuticals due to its chiral properties, enabling selective reactions in asymmetric synthesis. Employed in research for designing new drug candidates with improved metabolic stability and target specificity.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿2,900.00
inventory 250mg
10-20 days ฿5,320.00
inventory 1g
10-20 days ฿10,700.00

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1-(2,4-Difluorophenyl)ethanol
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Used as a key intermediate in the synthesis of antifungal agents, particularly in the production of fluconazole and related triazole antifungals. Its structure supports the formation of bioactive molecules that inhibit fungal cytochrome P450 enzymes, essential for ergosterol biosynthesis. Also utilized in the development of pharmaceuticals due to its chiral properties, enabling selective reactions in asymmetric synthesis. Employed in research for designing new drug candidates with improved metabolic stab

Used as a key intermediate in the synthesis of antifungal agents, particularly in the production of fluconazole and related triazole antifungals. Its structure supports the formation of bioactive molecules that inhibit fungal cytochrome P450 enzymes, essential for ergosterol biosynthesis. Also utilized in the development of pharmaceuticals due to its chiral properties, enabling selective reactions in asymmetric synthesis. Employed in research for designing new drug candidates with improved metabolic stability and target specificity.

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