519367
3,5-Bis(trifluoromethyl)benzenesulfonyl chloride
97%
Sign Into View Organizational & Contract Pricing
All Photos(1)
About This Item
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.)
functional group
fluoro
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
signalword
Danger
hcodes
Hazard Classifications
Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk_germany
WGK 3
flash_point_f
226.4 °F - closed cup
flash_point_c
108 °C - closed cup
ppe
Eyeshields, Faceshields, Gloves, type P3 (EN 143) respirator cartridges
Choose from one of the most recent versions:
Already Own This Product?
Find documentation for the products that you have recently purchased in the Document Library.
Customers Also Viewed
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.
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)
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)
Active Filters
Our team of scientists has experience in all areas of research including Life Science, Material Science, Chemical Synthesis, Chromatography, Analytical and many others.
Contact Technical Service
