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N-Bromosuccinimide or NBS is a chemical reagent used in radical substitution, electrophilic addition, and electrophilic substitution reactions in organic chemistry. NBS can be a convenient source of Br •, the bromine radical.
n-Bromosuccinimide (NBS) is a organobromide compound used in a variety of bromination reactions for chemical synthesis. It can be used to donate bromine to alkenes, to allylic or benzyl compounds, to carbonyl-containing compounds as well as aromatic compounds such as phenols, anilines, and various aromatic heterocycles.
N-Bromosuccinimide (NBS) is an organic compound commonly used as a brominating agent in organic synthesis. It is a convenient source of bromine radicals. It is used in radical bromination of allylic and benzylic positions.
N -Bromosuccinimide (NBS) is a brominating and oxidizing agent that is used as source for bromine in radical reactions (for example: allylic brominations) and various electrophilic additions.
N-Bromosuccinimide. N-Bromosuccinimide (NBS) is a highly specific bromination agent used in chemistry for both free-radical substitutions and electrophilic additions of unsaturated systems. It releases small quantities of bromine, which reacts with other compounds to facilitate the substitution reaction. From: Experimental Organic Chemistry, 2016
Jun 10, 2011 · N-Bromosuccinimide (NBS) As A Reagent In Organic Chemistry. In a blatant plug for the Reagent Guide, each Friday I profile a different reagent that is commonly encountered in Org 1/ Org 2. N-Bromosuccinimide Is A More Convenient Alternative To Bromine (Br 2)
N-Bromosuccinimide, better known as NBS, is a brominating and oxidizing agent widely used in organic chemistry. Despite its humble appearance as a white crystalline solid, NBS is responsible for catalyzing several critical transformations, making it a mainstay in the toolbox of organic chemists.
N-Bromosuccinimide. Molecular Formula C 4 H 4 BrNO 2; Average mass 177.984 Da; Monoisotopic mass 176.942535 Da; ChemSpider ID 60528
[Product Highlights] A Method for the Synthesis of Acyclic Haloamines with Ring Opening of Cyclic Amines. [Research Articles] Carbon-Heteroatom Bond Formation at the Benzylic Position of Methylarenes. [TCI Practical Example] Bromination Reaction Using N-Bromosuccinimide. Documents (Note: Some products will not have analytical charts available.)
Synonyms: NBS, N-Bromosuccinimide. CAS 128-08-5. Molecular Weight 177.98. Browse <I>N</I>-Bromosuccinimide and related products at Merck.
