794503
Ritter Trifluoroiodomethane-DMSO Reagent
Synonym(s):
2DMSO-CF3I, DMSO-trifluoromethyl iodide adduct
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About This Item
SMILES string
FC(F)(F)I.CS(C)=O.CS(C)=O
InChI
1S/2C2H6OS.CF3I/c2*1-4(2)3;2-1(3,4)5/h2*1-2H3;
InChI key
MMNWUCHAIFIKKV-UHFFFAOYSA-N
assay
95%
form
liquid
reaction suitability
reaction type: C-C Bond Formation
refractive index
n/D 1.466
density
1.529 at 25 °C
functional group
fluoro
iodo
sulfoxide
shipped in
dry ice
storage temp.
2-8°C
Application
signalword
Warning
hcodes
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
target_organs
Respiratory system
Storage Class
10 - Combustible liquids
wgk
WGK 3
flash_point_f
214.0 °F
flash_point_c
101.11 °C
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The Ritter lab currently focuses on fluorination chemistry for late-stage functionalization of complex natural and unnatural products. PhenoFluor™ has been developed as a general reagent for the selective, predictable, direct deoxyfluorination of complex alcohols and phenols.
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