3,4,5-trifluorothiophenol

98%

Reagent Code: #244860
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CAS Number 443683-18-9

science Other reagents with same CAS 443683-18-9

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scatter_plot Molecular Information
Weight 164.151 g/mol
Formula C₆H₃F₃S
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MDL Number MFCD11111065
inventory_2 Storage & Handling
Storage Room temperature

description Product Description

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds where enhanced metabolic stability and bioavailability are desired. Its fluorinated aromatic structure makes it valuable in medicinal chemistry for modifying drug candidates to improve their lipophilicity and binding affinity. Also employed in materials science for creating specialty polymers and liquid crystals with improved thermal and electronic properties due to the electron-withdrawing nature of fluorine atoms. Its thiol group allows for facile conjugation in molecular design, making it useful in the preparation of ligands for catalysis and functionalized surfaces.

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inventory 250mg
10-20 days ฿21,470.00

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3,4,5-trifluorothiophenol
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Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds where enhanced metabolic stability and bioavailability are desired. Its fluorinated aromatic structure makes it valuable in medicinal chemistry for modifying drug candidates to improve their lipophilicity and binding affinity. Also employed in materials science for creating specialty polymers and liquid crystals with improved thermal and electronic properties

Used as a key intermediate in the synthesis of pharmaceuticals and agrochemicals, particularly in the development of fluorinated organic compounds where enhanced metabolic stability and bioavailability are desired. Its fluorinated aromatic structure makes it valuable in medicinal chemistry for modifying drug candidates to improve their lipophilicity and binding affinity. Also employed in materials science for creating specialty polymers and liquid crystals with improved thermal and electronic properties due to the electron-withdrawing nature of fluorine atoms. Its thiol group allows for facile conjugation in molecular design, making it useful in the preparation of ligands for catalysis and functionalized surfaces.

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