N-氯邻磺酰苯甲酰亚胺
N-氯邻磺酰苯甲酰亚胺结构式
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常用名 | N-氯邻磺酰苯甲酰亚胺 | 英文名 | 2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide |
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| CAS号 | 14070-51-0 | 分子量 | 217.630 | |
| 密度 | 1.8±0.1 g/cm3 | 沸点 | 388.6±25.0 °C at 760 mmHg | |
| 分子式 | C7H4ClNO3S | 熔点 | 148-152ºC(lit.) | |
| MSDS | 中文版 美版 | 闪点 | 188.8±23.2 °C | |
| 符号 |
GHS07, GHS08 |
信号词 | Warning |
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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... |