3-(Pentafluoro-lambda6-sulfanyl)benzene-1-sulfonyl chloride

95%

Reagent Code: #227136
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CAS Number 1211520-62-5

science Other reagents with same CAS 1211520-62-5

blur_circular Chemical Specifications

scatter_plot Molecular Information
Weight 302.67 g/mol
Formula C₆H₄ClF₅O₂S₂
badge Registry Numbers
MDL Number MFCD16652436
inventory_2 Storage & Handling
Storage 2-8°C, Inert Gas

description Product Description

Used primarily as a fluorinating reagent in organic synthesis, this compound serves as a source of pentafluorosulfanyl (SF5) groups, which are highly electronegative and impart enhanced stability, lipophilicity, and metabolic resistance to pharmaceutical and agrochemical candidates. Its sulfonyl chloride functionality allows for easy incorporation into aromatic systems, making it valuable for constructing sulfone-containing molecules. It is employed in the development of specialty materials, including high-performance polymers and liquid crystals, where thermal and oxidative stability are critical. Due to the unique electronic properties of the SF5 group, it is also used in the design of energetic materials and functional molecules for medicinal chemistry research.

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Size Availability Unit Price Quantity
inventory 100mg
10-20 days ฿3,920.00
inventory 250mg
10-20 days ฿8,300.00
3-(Pentafluoro-lambda6-sulfanyl)benzene-1-sulfonyl chloride
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Used primarily as a fluorinating reagent in organic synthesis, this compound serves as a source of pentafluorosulfanyl (SF5) groups, which are highly electronegative and impart enhanced stability, lipophilicity, and metabolic resistance to pharmaceutical and agrochemical candidates. Its sulfonyl chloride functionality allows for easy incorporation into aromatic systems, making it valuable for constructing sulfone-containing molecules. It is employed in the development of specialty materials, including hi

Used primarily as a fluorinating reagent in organic synthesis, this compound serves as a source of pentafluorosulfanyl (SF5) groups, which are highly electronegative and impart enhanced stability, lipophilicity, and metabolic resistance to pharmaceutical and agrochemical candidates. Its sulfonyl chloride functionality allows for easy incorporation into aromatic systems, making it valuable for constructing sulfone-containing molecules. It is employed in the development of specialty materials, including high-performance polymers and liquid crystals, where thermal and oxidative stability are critical. Due to the unique electronic properties of the SF5 group, it is also used in the design of energetic materials and functional molecules for medicinal chemistry research.

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