2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide

2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide Structure
2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide structure
Common Name 2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide
CAS Number 14070-51-0 Molecular Weight 217.630
Density 1.8±0.1 g/cm3 Boiling Point 388.6±25.0 °C at 760 mmHg
Molecular Formula C7H4ClNO3S Melting Point 148-152ºC(lit.)
MSDS Chinese USA Flash Point 188.8±23.2 °C
Symbol GHS07 GHS08
GHS07, GHS08
Signal Word Warning

N-chlorosaccharin as a possible chlorinating reagent: structure, chlorine potential, and stability in water and organic solvents.

J. Pharm. Sci. 59(7) , 955-9, (1970)

Titrimetric determination of iodine-bromine numbers of some edible oils using three N-chloroimides.

J. Assoc. Off. Anal. Chem. 70(4) , 762-3, (1987)

Three simple titrimetric methods have been developed to determine iodine-bromine numbers of some edible oils, such as coconut, gingelly, groundnut, mustard, olive, palm olein, and sunflower, using 3 N-chloroimides. The 3 N-chloroimides are N-chlorophthalimide...

Ritter-type reactions of N-chlorosaccharin: a method for the electrophilic diamination of alkenes.

Org. Lett. 5(18) , 3313-5, (2003)

[reaction: see text] N-Chlorosaccharin has been shown to undergo electrophilic Ritter-type reactions with alkenes in acetonitrile. The resulting labile beta-chloro sulfonylamidines can be ring-opened and cyclized to imidazolines. Overall this provides a one p...