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・ N-Propyl chloride
・ N-Propyl iodide
・ N-Propyl-L-arginine
・ N-Reactor
・ N-red crown (n hieroglyph)
・ N-rule (Icelandic language)
・ N-SAT-110
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N-Bromosuccinimide
・ N-Butanol
・ N-Butylamine
・ N-Butyllithium
・ N-carbamoyl-D-amino acid hydrolase
・ N-carbamoyl-L-amino-acid hydrolase
・ N-carbamoylase
・ N-carbamoylputrescine amidase
・ N-carbamoylsarcosine amidase
・ N-category number
・ N-Chlorosuccinimide
・ N-class blimp
・ N-class ferry
・ N-Coded Music
・ N-connected


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N-Bromosuccinimide : ウィキペディア英語版
N-Bromosuccinimide

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''N''-Bromosuccinimide or NBS is a chemical reagent used in radical substitution and electrophilic addition reactions in organic chemistry. NBS can be a convenient source of Br•, the bromine radical.
==Preparation==
NBS is commercially available. It can also be synthesized in the laboratory. To do so, sodium hydroxide and bromine are added to an ice-water solution of succinimide. The NBS product precipitates out and can be collected by filtration.
Crude NBS gives better yield in the Wohl-Ziegler reaction. In other cases, impure NBS (slightly yellow in color) may give unreliable results. It can be purified by recrystallization from 90–95 °C water (10 g of NBS for 100 mL of water).

抄文引用元・出典: フリー百科事典『 ウィキペディア(Wikipedia)
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