4-(Trifluoromethoxy)benzyl alcohol

97%

Reagent Code: #240010
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Alias 4-(trifluoromethoxy)benzyl alcohol
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CAS Number 1736-74-9

science Other reagents with same CAS 1736-74-9

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 192.14 g/mol
Formula CF₃OC₆H₄CH₂OH
badge Registry Numbers
MDL Number MFCD00036029
thermostat Physical Properties
Boiling Point 108 °C25 mm Hg(lit.)
inventory_2 Storage & Handling
Density 1.326 g/mL at 25 °C(lit.)
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated compounds that exhibit enhanced metabolic stability and bioavailability. Its trifluoromethoxy group contributes to improved lipophilicity and electron-withdrawing properties, making it valuable in the design of active ingredients in crop protection agents and medicinal molecules. Commonly employed in the preparation of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) active drugs. Also utilized in the production of liquid crystals and functional materials where fluorinated building blocks are required for performance enhancement.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿500.00
inventory 5g
10-20 days ฿780.00
inventory 25g
10-20 days ฿2,540.00
inventory 100g
10-20 days ฿10,100.00
inventory 500g
10-20 days ฿45,390.00

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4-(Trifluoromethoxy)benzyl alcohol
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated compounds that exhibit enhanced metabolic stability and bioavailability. Its trifluoromethoxy group contributes to improved lipophilicity and electron-withdrawing properties, making it valuable in the design of active ingredients in crop protection agents and medicinal molecules. Commonly employed in the preparation of selective serotonin reuptake inhibitors (SSRIs) and other c

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated compounds that exhibit enhanced metabolic stability and bioavailability. Its trifluoromethoxy group contributes to improved lipophilicity and electron-withdrawing properties, making it valuable in the design of active ingredients in crop protection agents and medicinal molecules. Commonly employed in the preparation of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system (CNS) active drugs. Also utilized in the production of liquid crystals and functional materials where fluorinated building blocks are required for performance enhancement.

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