2,4,6-Triisopropylbenzenesulfonyl chloride
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What is the 2,4,6-Triisopropylbenzenesulfonyl chloride ?
2,4,6-Triisopropylbenzenesulfonyl chloride is White to cream solid, while it's Molecular Formula is C15H23ClO2S. 2,4,6-Triisopropylbenzenesulfonyl chloride can be used in the analysis of phosphonolipids in eggyolk by HPLC/MS technique. It can also be used to synthesize:Dimeric neomycin-neomycin conjugate with a flexible linker, 2,2′-(ethylenedioxy)bis(ethylamine).Coupling reagents for the synthesis of oligonucleotides.Sulfonates of pyrimidine nucleosides. These sulfonates can be displaced by nucleophiles in the presence of palladium-catalysts.
What is the CAS number for 2,4,6-Triisopropylbenzenesulfonyl chloride ?
The CAS number of 2,4,6-Triisopropylbenzenesulfonyl chloride is 6553-96-4.
More information of 2,4,6-Triisopropylbenzenesulfonyl chloride 6553-96-4 are:
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Synonyms |
2,4,6-Tris(1-methylethyl)benzenesulfonyl chloride;NSC 102803;Benzenesulfonylchloride, 2,4,6-triisopropyl- (6CI,7CI,8CI);2,4,6-Triisopropylphenylsulfonyl chloride; |
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CAS?Number |
6553-96-4 |
|
Molecular Formula |
C15H23ClO2S |
|
Molecular Weight |
302.865 |
|
Density |
1.096 g/cm3 |
|
Melting Point |
92-94 °C(lit.) |
|
Boiling Point |
349.3 °C at 760 mmHg |
|
Flash Point |
165.1 °C |
|
HS CODE |
29049020 |
|
PSA |
42.52000 |
|
LogP |
6.06510 |
What is 2,4,6-Triisopropylbenzenesulfonyl chloride (6553-96-4) used for?
2,4,6-Triisopropylbenzenesulfonyl chloride is an organic compound characterized by its triisopropylbenzene core and sulfonyl chloride functional group. It is a versatile reagent in organic synthesis and has unique properties due to its bulky isopropyl groups, which can influence its reactivity and selectivity in various chemical reactions.
InChI:InChI=1/C15H23ClO2S/c1-9(2)12-7-13(10(3)4)15(19(16,17)18)14(8-12)11(5)6/h7-11H,1-6H3
Articles related to 2,4,6-Triisopropylbenzenesulfonyl chloride:
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Article |
Source |
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Propanolysis of arenesulfonyl chlorides: Nucleophilic substitution at sulfonyl sulfur |
Iazykov, Mykyta,Canle, Moisés,Santaballa, J. Arturo,Rublova, Ludmila supporting information, (2017/09/08) |
|
Organocatalytic asymmetric mannich reactions of 5H-oxazol-4-ones: Highly enantio- and diastereoselective synthesis of chiral α-alkylisoserine derivatives |
Han, Zhiqiang,Yang, Wenguo,Tan, Choon-Hong,Jiang, Zhiyong , p. 1505 - 1511 (2013/06/27) |
How to get the best price on 2,4,6-Triisopropylbenzenesulfonyl chloride?
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