3-(Pentafluorosulfanyl)benzaldehyde

97%

Reagent Code: #227592
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CAS Number 401892-80-6

science Other reagents with same CAS 401892-80-6

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 232.17 g/mol
Formula C₇H₅F₅OS
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MDL Number MFCD03788517
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used primarily as a specialty intermediate in the synthesis of fluorinated organic compounds, particularly in pharmaceuticals and agrochemicals where high lipophilicity and metabolic stability are desired. Its pentafluorosulfanyl group imparts strong electron-withdrawing properties, making it valuable in the development of bioactive molecules with enhanced membrane permeability and resistance to oxidative degradation. It is also employed in materials science for designing novel fluorinated polymers and liquid crystals with unique thermal and dielectric properties. Due to the stability and distinct polarity of the SF5 group, this compound supports research in medicinal chemistry for structure-activity relationship studies, especially in aromatic systems targeting enzyme inhibitors or receptor ligands.

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Size Availability Unit Price Quantity
inventory 250mg
10-20 days ฿2,820.00
inventory 1g
10-20 days ฿8,050.00

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3-(Pentafluorosulfanyl)benzaldehyde
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Used primarily as a specialty intermediate in the synthesis of fluorinated organic compounds, particularly in pharmaceuticals and agrochemicals where high lipophilicity and metabolic stability are desired. Its pentafluorosulfanyl group imparts strong electron-withdrawing properties, making it valuable in the development of bioactive molecules with enhanced membrane permeability and resistance to oxidative degradation. It is also employed in materials science for designing novel fluorinated polymers and l

Used primarily as a specialty intermediate in the synthesis of fluorinated organic compounds, particularly in pharmaceuticals and agrochemicals where high lipophilicity and metabolic stability are desired. Its pentafluorosulfanyl group imparts strong electron-withdrawing properties, making it valuable in the development of bioactive molecules with enhanced membrane permeability and resistance to oxidative degradation. It is also employed in materials science for designing novel fluorinated polymers and liquid crystals with unique thermal and dielectric properties. Due to the stability and distinct polarity of the SF5 group, this compound supports research in medicinal chemistry for structure-activity relationship studies, especially in aromatic systems targeting enzyme inhibitors or receptor ligands.

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