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Names | |||
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Preferred IUPAC name
1-Chloropyrrolidine-2,5-dione | |||
Other names
Chlorosuccinimide
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Identifiers | |||
3D model (JSmol)
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Abbreviations | NCS | ||
113915 | |||
ChEBI | |||
ChEMBL | |||
ChemSpider | |||
ECHA InfoCard | 100.004.436 | ||
EC Number |
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122816 | |||
PubChem CID
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UNII | |||
CompTox Dashboard (EPA)
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Properties | |||
C4H4ClNO2 | |||
Molar mass | 133.53 g·mol−1 | ||
Appearance | white solid | ||
Density | 1.65 g/cm3 | ||
Melting point | 148 to 150 °C (298 to 302 °F; 421 to 423 K) | ||
Hazards | |||
GHS labelling: | |||
Danger | |||
H302, H314, H319, H335, H412 | |||
P260, P261, P264, P270, P271, P273, P280, P301+P312, P301+P330+P331, P303+P361+P353, P304+P340, P305+P351+P338, P310, P312, P321, P330, P337+P313, P363, P403+P233, P405, P501 | |||
Related compounds | |||
Related Imides
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Succinimide N-Bromosuccinimide N-Iodosuccinimide | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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N-Chlorosuccinimide ("NCS")is the organic compound with the formula C2H4(CO)2NCl. This white solid is used for chlorinations.[2] It is also used as a mild oxidant.[3] NCS is related to succinimide, but with N-Cl in place of N-H. The N–Cl bond is highly reactive, and NCS functions as a source of "Cl+".