2-(Trifluoromethoxy)aniline

Standard for GC, ≥99.9%(GC)

Reagent Code: #238122
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CAS Number 1535-75-7

science Other reagents with same CAS 1535-75-7

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 177.12 g/mol
Formula C₇H₆F₃NO
badge Registry Numbers
EC Number 216-257-9
MDL Number MFCD00035959
thermostat Physical Properties
Boiling Point 61-63 °C/15 mm Hg
inventory_2 Storage & Handling
Density 1.301 g/cm3
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its fluorinated aromatic structure which enhances bioavailability and metabolic stability. Also employed in the production of pharmaceuticals, where the trifluoromethoxy group contributes to improved lipophilicity and binding affinity. Additionally, it serves as a building block in the development of specialty polymers and liquid crystals, benefiting from the electron-withdrawing nature of the trifluoromethoxy moiety that influences molecular polarity and thermal stability.

Available Sizes & Pricing

Size Availability Unit Price Quantity
1g
10-20 days ฿1,280.00
2-(Trifluoromethoxy)aniline
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Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its fluorinated aromatic structure which enhances bioavailability and metabolic stability. Also employed in the production of pharmaceuticals, where the trifluoromethoxy group contributes to improved lipophilicity and binding affinity. Additionally, it serves as a building block in the development of specialty polymers and liquid crystals, benefiting from the electron-withdrawing nature of the t

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its fluorinated aromatic structure which enhances bioavailability and metabolic stability. Also employed in the production of pharmaceuticals, where the trifluoromethoxy group contributes to improved lipophilicity and binding affinity. Additionally, it serves as a building block in the development of specialty polymers and liquid crystals, benefiting from the electron-withdrawing nature of the trifluoromethoxy moiety that influences molecular polarity and thermal stability.

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