385417
3-(Trifluoromethyl)benzenesulfonyl chloride
Sign In to View Organizational & Contract Pricing.
Select a Size
About This Item
Linear Formula:
CF3C6H4SO2Cl
CAS Number:
Molecular Weight:
244.62
UNSPSC Code:
12352100
NACRES:
NA.22
PubChem Substance ID:
MDL number:
Beilstein/REAXYS Number:
2650774
Form:
liquid
InChI
1S/C7H4ClF3O2S/c8-14(12,13)6-3-1-2-5(4-6)7(9,10)11/h1-4H
SMILES string
FC(F)(F)c1cccc(c1)S(Cl)(=O)=O
InChI key
ONCAZCNPWWQQMW-UHFFFAOYSA-N
form
liquid
Quality Level
bp
88-90 °C/6 mmHg (lit.)
density
1.526 g/mL at 25 °C (lit.)
functional group
fluoro
Related Categories
signalword
Danger
hcodes
Hazard Classifications
Eye Dam. 1 - Skin Corr. 1B
Storage Class
8A - Combustible corrosive hazardous materials
wgk
WGK 3
flash_point_f
230.0 °F - closed cup
flash_point_c
110 °C - closed cup
ppe
Faceshields, Gloves, Goggles, type ABEK (EN14387) respirator filter
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.
Preparation of N-(a, ?-unsaturated acyl)-sulfonamides.
Katritzky et al.
ARKIVOC (Gainesville, FL, United States), 4, 115-124 (2009)
Synthesis, Characterization and Evaluation of Antibacterial Activity of Six Novel 1, 2, 4-Triazole Derivatives against Standard and Medical Bacteria.
Jacob et al.
Advanced Bacterial Genetics, Cold Spring Harbor, 5(6), 303-318 (2013)
Regiocontroled Palladium-Catalysed Direct Arylation at Carbon C2 of Benzofurans using Benzenesulfonyl Chlorides as the Coupling Partners.
Loukotova et al.
ChemCatChem, 5, 1303-1309 (2014)
Polymer supported reagents in synthesis: preparation of bicyclo[2.2.2] octane derivates via Tandem Michael addition reactions and subsequent combinatorial decoration.
S V Ley et al.
Journal of combinatorial chemistry, 2(2), 104-107 (2000-05-16)
Chemistry of aminophenols. Part 2: A general and efficient synthesis of indoles possessing a nitrogen substituent at the C4, C5, C6, and C7 positions.
Dai et al.
Tetrahedron Letters, 43, 7699-7702 (2002)
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