N-methyl-3-nitro-5-(trifluoromethyl)pyridin-2-amine

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Reagent Code: #219154
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CAS Number 175277-21-1

science Other reagents with same CAS 175277-21-1

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 221.14 g/mol
Formula C₇H₆F₃N₃O₂
badge Registry Numbers
MDL Number MFCD00068118
thermostat Physical Properties
Boiling Point 267.6±40.0 °C(Predicted)
inventory_2 Storage & Handling
Density 1.499±0.06 g/cm3(Predicted)
Storage Store at room temperature away from light

description Product Description

Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides. Its structure supports activity against certain plant pathogens and weed species, making it valuable in crop protection formulations. The compound’s nitro and trifluoromethyl groups enhance its reactivity and binding properties, contributing to improved efficacy and stability in final active ingredients. It is also explored in medicinal chemistry for potential bioactive molecule design due to its electron-withdrawing features and ability to influence metabolic stability.

shopping_cart Available Sizes & Pricing

Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿5,830.00
inventory 250mg
10-20 days ฿9,730.00
inventory 1g
10-20 days ฿16,340.00

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N-methyl-3-nitro-5-(trifluoromethyl)pyridin-2-amine
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Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides. Its structure supports activity against certain plant pathogens and weed species, making it valuable in crop protection formulations. The compound’s nitro and trifluoromethyl groups enhance its reactivity and binding properties, contributing to improved efficacy and stability in final active ingredients. It is also explored in medicinal chemistry for potential bioactiv
Used as an intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of herbicides and fungicides. Its structure supports activity against certain plant pathogens and weed species, making it valuable in crop protection formulations. The compound’s nitro and trifluoromethyl groups enhance its reactivity and binding properties, contributing to improved efficacy and stability in final active ingredients. It is also explored in medicinal chemistry for potential bioactive molecule design due to its electron-withdrawing features and ability to influence metabolic stability.
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