Ethyl 2-cyano-5-(trifluoromethyl)nicotinate

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Reagent Code: #184719
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CAS Number 1192263-82-3

science Other reagents with same CAS 1192263-82-3

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 244.17 g/mol
Formula C₁₀H₇F₃N₂O₂
badge Registry Numbers
MDL Number MFCD13193103
thermostat Physical Properties
Melting Point 55-57 °C
inventory_2 Storage & Handling
Storage Room temperature, seal, dry, light-proof

description Product Description

Used as a key intermediate in the synthesis of agrochemicals, particularly in the development of herbicides and insecticides. Featuring a cyano group at the 2-position and a trifluoromethyl group at the 5-position on a nicotinate scaffold, its structure allows for the introduction of fluorinated moieties, enhancing the bioavailability and metabolic stability of active ingredients. Also employed in medicinal chemistry for constructing nitrogen-containing heterocycles with potential pharmacological activity, such as enzyme inhibitors or modulators of cellular signaling. Commonly utilized in research settings for scaffold diversification in drug discovery programs.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿9,900.00
inventory 1g
10-20 days ฿27,870.00
inventory 100mg
10-20 days ฿6,190.00

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Ethyl 2-cyano-5-(trifluoromethyl)nicotinate
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Used as a key intermediate in the synthesis of agrochemicals, particularly in the development of herbicides and insecticides. Featuring a cyano group at the 2-position and a trifluoromethyl group at the 5-position on a nicotinate scaffold, its structure allows for the introduction of fluorinated moieties, enhancing the bioavailability and metabolic stability of active ingredients. Also employed in medicinal chemistry for constructing nitrogen-containing heterocycles with potential pharmacological activit

Used as a key intermediate in the synthesis of agrochemicals, particularly in the development of herbicides and insecticides. Featuring a cyano group at the 2-position and a trifluoromethyl group at the 5-position on a nicotinate scaffold, its structure allows for the introduction of fluorinated moieties, enhancing the bioavailability and metabolic stability of active ingredients. Also employed in medicinal chemistry for constructing nitrogen-containing heterocycles with potential pharmacological activity, such as enzyme inhibitors or modulators of cellular signaling. Commonly utilized in research settings for scaffold diversification in drug discovery programs.

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