N-Iodosuccinimide (NIS) is a reagent used in organic chemistry for the iodination of alkenes and as a mild oxidant.[2]
Quick Facts Names, Identifiers ...
N-Iodosuccinimide
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Names |
Preferred IUPAC name
1-Iodopyrrolidine-2,5-dione |
Identifiers |
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113917 |
ChEBI |
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ChemSpider |
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ECHA InfoCard |
100.007.475 |
EC Number |
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122896 |
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UNII |
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InChI=1S/C4H4INO2/c5-6-3(7)1-2-4(6)8/h1-2H2 Key: LQZMLBORDGWNPD-UHFFFAOYSA-N
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Properties |
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C4H4INO2 |
Molar mass |
224.985 g·mol−1 |
Appearance |
White solid |
Density |
2.245 g/cm3 |
Melting point |
202–206 °C (396–403 °F; 475–479 K)(dec.) [1] |
Solubility |
dioxane, THF, MeCN; insoluble in ether, CCl4 |
Hazards |
GHS labelling: |
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Warning |
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H302, H315, H319, H335 |
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P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P340, P305+P351+P338, P312, P321, P330, P332+P313, P337+P313, P362, P403+P233, P405, P501 |
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
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Close
NIS is the iodine analog of N-chlorosuccinimide (NCS) and N-bromosuccinimide (NBS) which are used for similar applications.