2,2,2-Trifluoroethanethiol

95%

Reagent Code: #242485
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CAS Number 1544-53-2

science Other reagents with same CAS 1544-53-2

blur_circular Chemical Specifications

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Weight 116.11 g/mol
Formula C₂H₃F₃S
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MDL Number MFCD00134386
inventory_2 Storage & Handling
Density 1.305 g/mL at 25 °C (lit.)
Storage Room temperature

description Product Description

Used primarily as a building block in organic synthesis, especially in the pharmaceutical and agrochemical industries. Its trifluoromethyl group enhances metabolic stability and lipophilicity in bioactive molecules, making it valuable for designing drugs with improved absorption and resistance to degradation. Commonly employed in the preparation of sulfide and disulfide derivatives, it participates in reactions with electrophiles to form carbon-sulfur bonds. Also utilized in the development of fluorinated specialty chemicals, including liquid crystals and functional materials, where the combination of fluorine and sulfur imparts unique electronic and physical properties.

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inventory 1g
10-20 days ฿10,430.00

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2,2,2-Trifluoroethanethiol
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Used primarily as a building block in organic synthesis, especially in the pharmaceutical and agrochemical industries. Its trifluoromethyl group enhances metabolic stability and lipophilicity in bioactive molecules, making it valuable for designing drugs with improved absorption and resistance to degradation. Commonly employed in the preparation of sulfide and disulfide derivatives, it participates in reactions with electrophiles to form carbon-sulfur bonds. Also utilized in the development of fluorinated s
Used primarily as a building block in organic synthesis, especially in the pharmaceutical and agrochemical industries. Its trifluoromethyl group enhances metabolic stability and lipophilicity in bioactive molecules, making it valuable for designing drugs with improved absorption and resistance to degradation. Commonly employed in the preparation of sulfide and disulfide derivatives, it participates in reactions with electrophiles to form carbon-sulfur bonds. Also utilized in the development of fluorinated specialty chemicals, including liquid crystals and functional materials, where the combination of fluorine and sulfur imparts unique electronic and physical properties.
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