Methyl 6-(2,2,2-trifluoroethoxy)nicotinate

95%

Reagent Code: #49436
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CAS Number 287979-27-5

science Other reagents with same CAS 287979-27-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 235.1599 g/mol
Formula C₉H₈F₃NO₃
badge Registry Numbers
MDL Number MFCD00831623
thermostat Physical Properties
Boiling Point 241.2 °C at 760 mmHg
inventory_2 Storage & Handling
Density 1.325g/cm3
Storage room temperature

description Product Description

This chemical is primarily used in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of drugs that target specific biological pathways, often in the treatment of metabolic and neurological disorders. Its trifluoroethoxy group enhances the stability and bioavailability of the resulting drug molecules, making it valuable in medicinal chemistry. Additionally, it is utilized in research settings for the development of novel therapeutic agents, especially in the field of organic synthesis and drug discovery.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,411.00

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Methyl 6-(2,2,2-trifluoroethoxy)nicotinate
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This chemical is primarily used in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of drugs that target specific biological pathways, often in the treatment of metabolic and neurological disorders. Its trifluoroethoxy group enhances the stability and bioavailability of the resulting drug molecules, making it valuable in medicinal chemistry. Additionally, it is utilized in research set

This chemical is primarily used in the synthesis of pharmaceutical compounds, particularly in the development of active pharmaceutical ingredients (APIs). It serves as a key intermediate in the production of drugs that target specific biological pathways, often in the treatment of metabolic and neurological disorders. Its trifluoroethoxy group enhances the stability and bioavailability of the resulting drug molecules, making it valuable in medicinal chemistry. Additionally, it is utilized in research settings for the development of novel therapeutic agents, especially in the field of organic synthesis and drug discovery.

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