Weight | 177.985 g/mol |
---|---|
Formula | C4H4BrNO2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 0 |
Rotatable Bonds | 0 |
N-Bromosuccinimide (128-08-5)
Bromosuccinimide · Succinbromimide · N Bromosuccinimide
Score:
#1767 in Physics
,
#2112 in Biochemistry
,
#5502 in Chemistry
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- [58] Determination of the tryptophan content of proteins with N-bromosuccinimide (Methods in Enzymology, 1967)
- Brominations with N-Bromosuccinimide and Related Compounds. The Wohl-Ziegler Reaction. (Chemical Reviews, 1948)
- N-Bromosuccinimide-dimethylformamide: a mild, selective nuclear monobromination reagent for reactive aromatic compounds (Journal of Organic Chemistry, 1979)
- Reaction of O-benzylidene sugars with N-bromosuccinimide. II. Scope and synthetic utility in the methyl 4,6-0-benzylidenehexopyranoside series (Journal of Organic Chemistry, 1969)
- Oxidations and Dehydrogenations with N-Bromosuccinimide and Related N-Haloimides. (Chemical Reviews, 1963)
- Selective Oxidation with N-Bromosuccinimide. II. Cholestane-3,5,6-triol (Journal of the American Chemical Society, 1949)
-
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - Bromosuccinimide
- Succinbromimide
- N Bromosuccinimide
-
SMILESC1CC(=O)N(C1=O)Br
-
InChIKeyPCLIMKBDDGJMGD-UHFFFAOYSA-N
- Pubchem - N-Bromosuccinimide
- Wikipedia - N-bromosuccinimide
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.
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