![]() 2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide structure
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Common Name | 2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide | ||
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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 |
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)
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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... |
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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... |
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