4-(Trifluoromethylthio)benzaldehyde

90%

Reagent Code: #240040
label
Alias 4-(trifluoromethylthio)benzaldehyde; p-trifluoromethylthiobenzaldehyde
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CAS Number 4021-50-5

science Other reagents with same CAS 4021-50-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 206.18 g/mol
Formula C₈H₅F₃OS
badge Registry Numbers
MDL Number MFCD00129191
thermostat Physical Properties
Melting Point 29-31 °C(lit.)
Boiling Point 219 °C(lit.)
inventory_2 Storage & Handling
Density 1.31 g/cm3
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals due to the presence of both aldehyde and trifluoromethylthio groups. The aldehyde functionality allows for easy derivatization, such as condensation reactions to form imines or oximes, or reduction to alcohol. The trifluoromethylthio group enhances lipophilicity and metabolic stability, making this compound valuable in the development of bioactive molecules. Commonly employed in medicinal chemistry for constructing drug candidates targeting central nervous system disorders, antimicrobial agents, and anti-inflammatory compounds. Also utilized in the preparation of functional materials and ligands for catalysis.

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Size Availability Unit Price Quantity
inventory 5g
10-20 days ฿3,020.00
inventory 25g
10-20 days ฿10,800.00
inventory 1g
10-20 days ฿800.00

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4-(Trifluoromethylthio)benzaldehyde
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals due to the presence of both aldehyde and trifluoromethylthio groups. The aldehyde functionality allows for easy derivatization, such as condensation reactions to form imines or oximes, or reduction to alcohol. The trifluoromethylthio group enhances lipophilicity and metabolic stability, making this compound valuable in the development of bioactive molecules. Commonly employed in medicinal chemistry for constructing drug cand

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals due to the presence of both aldehyde and trifluoromethylthio groups. The aldehyde functionality allows for easy derivatization, such as condensation reactions to form imines or oximes, or reduction to alcohol. The trifluoromethylthio group enhances lipophilicity and metabolic stability, making this compound valuable in the development of bioactive molecules. Commonly employed in medicinal chemistry for constructing drug candidates targeting central nervous system disorders, antimicrobial agents, and anti-inflammatory compounds. Also utilized in the preparation of functional materials and ligands for catalysis.

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