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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
Regulatory Listings
Regulatory Listings are mainly provided for chemical products. Only limited information can be provided here for non-chemical products. No entry means none of the components are listed. It is the user’s obligation to ensure the safe and legal use of the product.
JAN Code
ALD00062-VAR:
ALD00062-BULK:
ALD00062-10G:
ALD00062-1G:
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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.
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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