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![1-Chloromethyl-4-fluoro-1,4-diazoniabicyclo[2.2.2]octane bis(tetrafluoroborate) >95% in F+ active](/deepweb/assets/sigmaaldrich/product/structures/206/487/53d52ee5-ef71-4e9a-9bc8-938b68b98d5d/640/53d52ee5-ef71-4e9a-9bc8-938b68b98d5d.png)
Quality Level
Assay
95%
form
solid
reaction suitability
reaction type: click chemistry
mp
30-36 °C
SMILES string
FS(C1=C(F)C=CC(F)=C1)(=O)=O
InChI
1S/C6H3F3O2S/c7-4-1-2-5(8)6(3-4)12(9,10)11/h1-3H
InChI key
QHGFXAZDLIJQIV-UHFFFAOYSA-N
Application
acids. This new click chemistry approach through sulfates is a complimentary approach to using amides and phosphate groups as linkers.
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
Storage Class Code
8A - Combustible corrosive hazardous materials
WGK
WGK 3
Flash Point(F)
216.0 °F
Flash Point(C)
102.22 °C
Certificates of Analysis (COA)
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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.
In collaboration with K. Barry Sharpless and coworkers, we offer a variety of sulfonyl fluoride reagents that undergo a “Click II” reaction.
In collaboration with K. Barry Sharpless and coworkers, we offer a variety of sulfonyl fluoride reagents that undergo a “Click II” reaction.
In collaboration with K. Barry Sharpless and coworkers, we offer a variety of sulfonyl fluoride reagents that undergo a “Click II” reaction.
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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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