(Trifluoromethoxy)benzene

99%

Reagent Code: #239604
label
Alias α,α,α-trifluoroanisole, phenyltrifluoromethyl ether
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CAS Number 456-55-3

science Other reagents with same CAS 456-55-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 162.11 g/mol
Formula C₇H₅F₃O
badge Registry Numbers
EC Number 207-269-5
MDL Number MFCD00040832
thermostat Physical Properties
Boiling Point 102 °C(lit.)
inventory_2 Storage & Handling
Density 1.226 g/mL at 25 °C(lit.)
Storage Room temperature, flammable area

description Product Description

Used as a building block in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds requiring enhanced metabolic stability and lipophilicity. Its trifluoromethoxy group contributes to improved bioavailability and resistance to oxidative degradation, making it valuable in medicinal chemistry. Also employed in the manufacture of liquid crystals and functional materials due to its unique electronic and steric properties. Commonly utilized in fluorinated analog design to modulate the potency and pharmacokinetics of active ingredients.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿290.00
inventory 100g
10-20 days ฿1,120.00
inventory 500g
10-20 days ฿5,160.00
inventory 25g
10-20 days ฿330.00
inventory 2.5kg
10-20 days ฿20,520.00

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(Trifluoromethoxy)benzene
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Used as a building block in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds requiring enhanced metabolic stability and lipophilicity. Its trifluoromethoxy group contributes to improved bioavailability and resistance to oxidative degradation, making it valuable in medicinal chemistry. Also employed in the manufacture of liquid crystals and functional materials due to its unique electronic and steric properties. Commonly utilized in fluorinated analog design to
Used as a building block in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of compounds requiring enhanced metabolic stability and lipophilicity. Its trifluoromethoxy group contributes to improved bioavailability and resistance to oxidative degradation, making it valuable in medicinal chemistry. Also employed in the manufacture of liquid crystals and functional materials due to its unique electronic and steric properties. Commonly utilized in fluorinated analog design to modulate the potency and pharmacokinetics of active ingredients.
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