Weight | 302.867 g/mol |
---|---|
Formula | C15H23ClO2S |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 4 |
2,4,6-Triisopropylbenzenesulfonyl chloride (6553-96-4)
2,4,6-triisopropylbenzenesulfonyl · 2,4,6-TIPBS
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- Studies on Polynucleotides. LII.1 The Use of 2,4,6-Triisopropylbenzenesulfonyl Chloride for the Synthesis of Internucleotide Bonds2 (Journal of the American Chemical Society, 1966)
- Mono-6-(O-2,4,6-triisopropylbenzenesulfonyl)--cyclodextrin, a novel intermediate for the synthesis of mono-functionalised -cyclodextrins (Tetrahedron Letters, 2001)
- A new condensing reagent, 1-(2,4,6-triisopropylbenzenesulfonyl)-5-(pyridin-2-yl)tetrazolide and its use in the synthesis of cro binding heptadecanucleotide on a polymer support (Nucleic Acids Research, 1982)
- TwoStep Syntheses of 2,4,6Triisopropylbenzenesulfonyl Aziridines. (Tetrahedron Letters, 2005)
- A 31p NMR study of the reaction of adenosine 3,5-cyclic monophosphate with 2,4,6-triisopropylbenzenesulfonyl chloride (Nucleosides, Nucleotides & Nucleic Acids, 1987)
- Unexpected Sultine Formation Resulting from the Friedel-Crafts Sulfonylation of Fluorene with 2,4,6-Triisopropylbenzenesulfonyl Chloride (Synthetic Communications, 1990)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - 2,4,6-triisopropylbenzenesulfonyl
- 2,4,6-TIPBS
-
SMILESCC(C)C1=CC(=C(C(=C1)C(C)C)S(=O)(=O)Cl)C(C)C
-
InChIKeyJAPYIBBSTJFDAK-UHFFFAOYSA-N
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Synthesis
Reactant
+
2-CHLOROPROPANE
(Friedel-Crafts alkylation)
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