Name: N-chlorosuccinimide
English name: N-Chlorosuccinimide
Other name: N-chlorosuccinimide N-chlorosuccinimide succinyl chloride imine succinyl chloride imide
Chemical formula: C4H4ClNO2
Molecular weight: 133.53
Melting point: 144-150℃
Closeness 1.5g/cm3
EINECS:204-878-8
Melting point: 144-150℃
Relative density: 1.5g/cm3
use
1. An important chlorinating agent that can chlorinate aromatic aldehydes without affecting the aromatic ring. In the chlorination of aniline and N-alkylaniline (mainly ortho), the chlorination of a-aminopyridine, the dehydrochlorination and degradation chlorination of a-phenylthioamide, and the monochlorination of cyclopentadiene Both have higher yields than chlorine, tert-butyl hypochlorite, and chloramine T. As oxidants, diols can be oxidized to lactones, primary (secondary) alcohols are oxidized to aldehydes (ketones), and B-hydroxyketones are oxidized to B-diketones. It can selectively break the peptide bond formed by tryptophan under acidic conditions. It can also be used in the synthesis of allylamine, B, R-unsaturated amino acids and their derivatives.
2. Pharmaceutical intermediates. Commonly used in the synthesis of antibiotics, such as benzyl cephalosporin, can also be used to prepare rubber additives.
3. N-chlorosuccinimide (NCS) is a convenient electrophilic addition and electrophilic substitution reagent, commonly used in the chlorination of sulfides, sulfones and ketones, and can also be used to synthesize N-chlorine amines .
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