3,5-Bis(trifluoromethyl)benzene-1-sulfonyl chloride
3,5-Bis(trifluoromethyl)benzene-1-sulfonyl chloride structure
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Common Name | 3,5-Bis(trifluoromethyl)benzene-1-sulfonyl chloride | ||
|---|---|---|---|---|
| CAS Number | 39234-86-1 | Molecular Weight | 312.617 | |
| Density | 1.6±0.1 g/cm3 | Boiling Point | 248.3±40.0 °C at 760 mmHg | |
| Molecular Formula | C8H3ClF6O2S | Melting Point | 34-38 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 104.0±27.3 °C | |
| Symbol |
GHS05 |
Signal Word | Danger | |
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New library of aminosulfonyl-tagged Hoveyda-Grubbs type complexes: Synthesis, kinetic studies and activity in olefin metathesis transformations.
Beilstein J. Org. Chem. 6 , 1159-66, (2010) Seven novel Hoveyda-Grubbs precatalysts bearing an aminosulfonyl function are reported. Kinetic studies indicate an activity enhancement compared to Hoveyda's precatalyst. A selection of these catalysts was investigated with various substrates in ring-closing... |
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Highly enantioselective catalytic thiolysis of prochiral cyclic dicarboxylic anhydrides utilizing a bifunctional chiral sulfonamide.
Angew. Chem. Int. Ed. Engl. 44(36) , 5838-41, (2005)
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Versatile chiral reagent for the highly enantioselective synthesis of either anti or syn ester aldols. Corey EJ and Kim SS.
J. Am. Chem. Soc. 112(12) , 4976-4977, (1990)
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Protein diffusion in porous gel filtration chromatography media studied by pulsed field gradient NMR spectroscopy. Gibbs SJ, et al.
J. Phys. Chem. 96(18) , 7458-7462, (1992)
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