ALD00158
5-Chloro-2-thiophenesulfonyl fluoride
95%
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About This Item
Quality Level
Assay
95%
form
liquid
reaction suitability
reaction type: click chemistry
refractive index
n20/D 1.529
density
1.571 g/mL at 25 °C
SMILES string
ClC1=CC=C(S(F)(=O)=O)S1
InChI
1S/C4H2ClFO2S2/c5-3-1-2-4(9-3)10(6,7)8/h1-2H
InChI key
XZQCGAGVTAESGC-UHFFFAOYSA-N
Related Categories
Application
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
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。
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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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