2-Chloro-6-nitro-4-(trifluoromethyl)aniline

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Reagent Code: #164087
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CAS Number 57729-79-0

science Other reagents with same CAS 57729-79-0

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 240.57 g/mol
Formula C₇H₄ClF₃N₂O₂
badge Registry Numbers
MDL Number MFCD00042153
thermostat Physical Properties
Melting Point 66-68 °C
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof

description Product Description

Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its structure allows for further functionalization, making it valuable in creating active ingredients that target specific plant pathogens or pests. Also employed in research settings for the preparation of dyes and fluorescent compounds due to its electron-withdrawing groups and aromatic backbone. The presence of chlorine, nitro, and trifluoromethyl groups enhances reactivity and binding properties in complex organic transformations.

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Test Parameter Specification
Appearance Light Yellow to Yellow Solid
Purity 97.5-100
Infrared Spectrum Conforms to Structure
NMR Conforms to Structure

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿1,290.00
inventory 5g
10-20 days ฿4,560.00
inventory 25g
10-20 days ฿10,390.00

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2-Chloro-6-nitro-4-(trifluoromethyl)aniline
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Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its structure allows for further functionalization, making it valuable in creating active ingredients that target specific plant pathogens or pests. Also employed in research settings for the preparation of dyes and fluorescent compounds due to its electron-withdrawing groups and aromatic backbone. The presence of chlorine, nitro, and trifluoromethyl groups enhances re
Used as an intermediate in the synthesis of agrochemicals and pharmaceuticals, particularly in the development of herbicides and fungicides. Its structure allows for further functionalization, making it valuable in creating active ingredients that target specific plant pathogens or pests. Also employed in research settings for the preparation of dyes and fluorescent compounds due to its electron-withdrawing groups and aromatic backbone. The presence of chlorine, nitro, and trifluoromethyl groups enhances reactivity and binding properties in complex organic transformations.
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