| Weight | 133.534 g/mol |
|---|---|
| Formula | C4H4ClNO2 |
| Hydrogen Acceptors | 2 |
| Hydrogen Donors | 0 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 0 |
N-CHLOROSUCCINIMIDE (128-09-6)
Score:
#1254 in Biochemistry
,
#1335 in Physics
,
#3874 in Chemistry
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- A new method for partial peptide mapping using N-chlorosuccinimide/urea and peptide silver staining in sodium dodecyl sulfate-polyacrylamide gels. (Analytical Biochemistry, 1982)
- Efficient and highly selective oxidation of primary alcohols to aldehydes by N-chlorosuccinimide mediated by oxoammonium salts (Journal of Organic Chemistry, 1996)
- N-chlorosuccinimide-promoted regioselective sulfenylation of imidazoheterocycles at room temperature. (Organic Letters, 2014)
- Halogenation of Aromatic Compounds by N-Bromo- and N-Chlorosuccinimide under Ionic Conditions (Journal of Organic Chemistry, 1965)
- Selective chemical cleavage of tryptophanyl peptide bonds by oxidative chlorination with N-chlorosuccinimide. (Biochemistry, 1976)
- Efficient .alpha.-halogenation of acyl chlorides by N-bromosuccinimide, N-chlorosuccinimide, and molecular iodine (Journal of Organic Chemistry, 1975)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1CC(=O)N(C1=O)Cl
-
InChIKeyJRNVZBWKYDBUCA-UHFFFAOYSA-N
- Pubchem - N-CHLOROSUCCINIMIDE
- Wikipedia - N-chlorosuccinimide
N-Chlorosuccinimide is used for chlorinations and as a mild oxidant. N-Iodosuccinimide (NIS), the iodine analog of N-chlorosuccinimide, and N-bromosuccinimide (NBS), the bromine analog, are used for similar applications.
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N-CHLOROSUCCINIMIDE
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