519367
3,5-Bis(trifluoromethyl)benzenesulfonyl chloride
97%
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Linear Formula:
(CF3)2C6H3SO2Cl
CAS Number:
Molecular Weight:
312.62
EC Number:
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
Recommended Products
Assay
97%
mp
34-38 °C (lit.)
SMILES string
FC(F)(F)c1cc(cc(c1)S(Cl)(=O)=O)C(F)(F)F
InChI
1S/C8H3ClF6O2S/c9-18(16,17)6-2-4(7(10,11)12)1-5(3-6)8(13,14)15/h1-3H
InChI key
BTRCVKADYDVSLI-UHFFFAOYSA-N
Signal Word
Danger
Hazard Statements
Precautionary Statements
Hazard Classifications
Skin Corr. 1B
WGK
WGK 3
Flash Point(F)
226.4 °F
Flash Point(C)
108 °C
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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Protein diffusion in porous gel filtration chromatography media studied by pulsed field gradient NMR spectroscopy.
Gibbs SJ, et al.
The Journal of Physical Chemistry, 96(18), 7458-7462 (1992)
Versatile chiral reagent for the highly enantioselective synthesis of either anti or syn ester aldols.
Corey EJ and Kim SS.
Journal of the American Chemical Society, 112(12), 4976-4977 (1990)
Highly enantioselective catalytic thiolysis of prochiral cyclic dicarboxylic anhydrides utilizing a bifunctional chiral sulfonamide.
Takashi Honjo et al.
Angewandte Chemie (International ed. in English), 44(36), 5838-5841 (2005-08-05)
Etienne Borré et al.
Beilstein journal of organic chemistry, 6, 1159-1166 (2010-12-18)
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 metathesis of dienes or enynes and cross metathesis.
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