6-(2,2,2-Trifluoroethoxy)nicotinaldehyde

98%

Reagent Code: #120398
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CAS Number 159981-19-8

science Other reagents with same CAS 159981-19-8

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 205.13 g/mol
Formula C₈H₆F₃NO₂
badge Registry Numbers
MDL Number MFCD06738679
thermostat Physical Properties
Boiling Point 239.8°C at 760 mmHg
inventory_2 Storage & Handling
Storage 2-8°C, store under inert gas

description Product Description

Used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the production of compounds with potential biological activity. Its trifluoroethoxy group enhances the lipophilicity and metabolic stability of the resulting molecules, making it valuable in drug discovery. It is also employed in the synthesis of heterocyclic compounds, which are crucial in medicinal chemistry for designing new therapeutic agents. Additionally, its aldehyde functionality allows for further functionalization, enabling the creation of diverse chemical structures for research and industrial applications.

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Size Availability Unit Price Quantity
inventory 1g
10-20 days ฿4,815.00
inventory 250mg
10-20 days ฿2,007.00
inventory 100mg
10-20 days ฿1,404.00
inventory 5g
10-20 days ฿18,063.00

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6-(2,2,2-Trifluoroethoxy)nicotinaldehyde
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Used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the production of compounds with potential biological activity. Its trifluoroethoxy group enhances the lipophilicity and metabolic stability of the resulting molecules, making it valuable in drug discovery. It is also employed in the synthesis of heterocyclic compounds, which are crucial in medicinal chemistry for designing new therapeutic agents. Additionally, its aldehyde

Used in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals. It serves as a key intermediate in the production of compounds with potential biological activity. Its trifluoroethoxy group enhances the lipophilicity and metabolic stability of the resulting molecules, making it valuable in drug discovery. It is also employed in the synthesis of heterocyclic compounds, which are crucial in medicinal chemistry for designing new therapeutic agents. Additionally, its aldehyde functionality allows for further functionalization, enabling the creation of diverse chemical structures for research and industrial applications.

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