4-Hydroxy-3-(trifluoromethyl)benzaldehyde

98%

Reagent Code: #193784
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CAS Number 220227-98-5

science Other reagents with same CAS 220227-98-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 190.12 g/mol
Formula C₈H₅F₃O₂
badge Registry Numbers
MDL Number MFCD01091006
thermostat Physical Properties
Melting Point 159-163°C
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. Its structure supports the formation of bioactive molecules due to the presence of both aldehyde and hydroxyl functional groups, which allow for further chemical modifications. Commonly employed in the development of fluorinated organic compounds, where the trifluoromethyl group enhances metabolic stability and lipophilicity. Also utilized in agrochemicals for creating herbicides and fungicides, benefiting from the electron-withdrawing properties of the trifluoromethyl group that improve environmental stability. Serves as a building block in liquid crystal materials and organic semiconductors due to its rigid aromatic framework and polar substituents.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿495.00
inventory 1g
10-20 days ฿1,078.00

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4-Hydroxy-3-(trifluoromethyl)benzaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals, particularly in the production of selective serotonin reuptake inhibitors (SSRIs) and other central nervous system agents. Its structure supports the formation of bioactive molecules due to the presence of both aldehyde and hydroxyl functional groups, which allow for further chemical modifications. Commonly employed in the development of fluorinated organic compounds, where the trifluoromethyl group enhances metabolic stability and lipophilicity. Also utilized in agrochemicals for creating herbicides and fungicides, benefiting from the electron-withdrawing properties of the trifluoromethyl group that improve environmental stability. Serves as a building block in liquid crystal materials and organic semiconductors due to its rigid aromatic framework and polar substituents.
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