5-Methyl-2-(trifluoromethoxy)aniline

≥95%

Reagent Code: #202893
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CAS Number 151276-15-2

science Other reagents with same CAS 151276-15-2

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 191.15 g/mol
Formula C₈H₈F₃NO
badge Registry Numbers
MDL Number MFCD18399696
inventory_2 Storage & Handling
Storage Room temperature, light-proof, inert gas

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 development of pharmaceuticals where the trifluoromethoxy group contributes to improved lipophilicity and binding affinity. Its amine functionality allows for easy derivatization, making it valuable in medicinal chemistry for constructing more complex molecules. Additionally, it finds use in the preparation of dyes and functional materials requiring thermal and chemical resistance.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿14,740.00
inventory 1g
10-20 days ฿39,730.00
inventory 5g
10-20 days ฿139,040.00
5-Methyl-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 development of pharmaceuticals where the trifluoromethoxy group contributes to improved lipophilicity and binding affinity. Its amine functionality allows for easy derivatization, making it valuable in medicinal chemistry for constructing more complex molecules. Additionally, it finds

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 development of pharmaceuticals where the trifluoromethoxy group contributes to improved lipophilicity and binding affinity. Its amine functionality allows for easy derivatization, making it valuable in medicinal chemistry for constructing more complex molecules. Additionally, it finds use in the preparation of dyes and functional materials requiring thermal and chemical resistance.

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