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About This Item
Product Name
4-Chlorobenzenesulfonyl fluoride, 95%
form
solid
InChI
1S/C6H4ClFO2S/c7-5-1-3-6(4-2-5)11(8,9)10/h1-4H
SMILES string
ClC1=CC=C(S(=O)(F)=O)C=C1
InChI key
PCTLRVPDZBVCMP-UHFFFAOYSA-N
assay
95%
reaction suitability
reaction type: click chemistry
mp
45-50 °C
Quality Level
Related Categories
Application
This new click chemistry approach through sulfates is a complimentary approach to using amides and phosphate groups as linkers.
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
Regulatory Information
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Articles
In collaboration with K. Barry Sharpless and coworkers, we offer a variety of sulfonyl fluoride reagents that undergo a “Click II” reaction.
This article details the latest progress in synthesizing alkylsulfonyl fluorides through different approaches that utilize photoredox catalysis, electrocatalysis, transition-metal catalysis, and organocatalysis. The alkylsulfonyl fluorides thus prepared could be utilized further in sulfur(VI) fluoride exchange (SuFEx) click reactions.
在与K. Barry Sharpless及其同事合作后,Sigma-Aldrich现可提供各种磺酰氟试剂,这些试剂经历了“Click II”反应。
Related Content
The Sharpless Lab pursues useful new reactivity and general methods for selectively controlling chemical reactions.
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
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