1-(2-(Difluoromethoxy)phenyl)ethan-1-amine

95%

Reagent Code: #167306
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CAS Number 144759-10-4

science Other reagents with same CAS 144759-10-4

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 187.18 g/mol
Formula C₉H₁₁NOF₂
badge Registry Numbers
MDL Number MFCD02689995
thermostat Physical Properties
Boiling Point 240.8±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.155±0.06 g/cm3(Predicted)
Storage 2-8°C, light-proof, inert gas

description Product Description

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of bioactive molecules with enhanced metabolic stability and membrane permeability. Its structure supports the design of compounds targeting central nervous system disorders due to favorable lipophilicity and resistance to oxidative degradation. Also employed in agrochemicals for creating herbicides and fungicides where fluorine substitution improves environmental persistence and target selectivity. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies involving amine-containing analogs.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿10,710.00
inventory 1g
10-20 days ฿50,580.00

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1-(2-(Difluoromethoxy)phenyl)ethan-1-amine
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Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of bioactive molecules with enhanced metabolic stability and membrane permeability. Its structure supports the design of compounds targeting central nervous system disorders due to favorable lipophilicity and resistance to oxidative degradation. Also employed in agrochemicals for creating herbicides and fungicides where fluorine substitution improves environmental persistence and target selectivity

Used as a key intermediate in the synthesis of fluorinated pharmaceuticals, particularly in the development of bioactive molecules with enhanced metabolic stability and membrane permeability. Its structure supports the design of compounds targeting central nervous system disorders due to favorable lipophilicity and resistance to oxidative degradation. Also employed in agrochemicals for creating herbicides and fungicides where fluorine substitution improves environmental persistence and target selectivity. Commonly utilized in medicinal chemistry for structure-activity relationship (SAR) studies involving amine-containing analogs.

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