3-Methyl-4-(trifluoromethyl)aniline

98%

Reagent Code: #214332
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CAS Number 106877-31-0

science Other reagents with same CAS 106877-31-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 175.15 g/mol
Formula C₈H₈F₃N
badge Registry Numbers
MDL Number MFCD18399852
inventory_2 Storage & Handling
Storage 2-8°C, sealed, dry, light-proof

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 bioactivity and stability. Also employed in the production of pharmaceuticals where the trifluoromethyl group contributes to improved metabolic resistance and binding affinity. Additionally, it serves as a building block in the development of specialty polymers and dyes, where its amine functionality allows for coupling reactions and structural modification.

Available Sizes & Pricing

Size Availability Unit Price Quantity
100mg
10-20 days ฿3,080.00
250mg
10-20 days ฿3,970.00
1g
10-20 days ฿8,480.00
3-Methyl-4-(trifluoromethyl)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 bioactivity and stability. Also employed in the production of pharmaceuticals where the trifluoromethyl group contributes to improved metabolic resistance and binding affinity. Additionally, it serves as a building block in the development of specialty polymers and dyes, where its amine functionality allows for coupling reactions and structural m

Used as a key intermediate in the synthesis of agrochemicals, particularly herbicides and insecticides, due to its fluorinated aromatic structure which enhances bioactivity and stability. Also employed in the production of pharmaceuticals where the trifluoromethyl group contributes to improved metabolic resistance and binding affinity. Additionally, it serves as a building block in the development of specialty polymers and dyes, where its amine functionality allows for coupling reactions and structural modification.

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