452742
N-Chlorosaccharin
99%
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About This Item
Empirical Formula (Hill Notation):
C7H4ClNO3S
CAS Number:
Molecular Weight:
217.63
NACRES:
NA.22
PubChem Substance ID:
UNSPSC Code:
12352100
MDL number:
Assay:
99%
Product Name
N-Chlorosaccharin, 99%
InChI
1S/C7H4ClNO3S/c8-9-7(10)5-3-1-2-4-6(5)13(9,11)12/h1-4H
SMILES string
ClN1C(=O)c2ccccc2S1(=O)=O
InChI key
VKWMGUNWDFIWNW-UHFFFAOYSA-N
assay
99%
mp
148-152 °C (lit.)
signalword
Warning
hcodes
Hazard Classifications
Acute Tox. 4 Oral - Carc. 2
Storage Class
11 - Combustible Solids
wgk
WGK 3
flash_point_f
Not applicable
flash_point_c
Not applicable
ppe
dust mask type N95 (US), Eyeshields, Gloves
Regulatory Information
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N-chlorosaccharin as a possible chlorinating reagent: structure, chlorine potential, and stability in water and organic solvents.
H S Dawn et al.
Journal of pharmaceutical sciences, 59(7), 955-959 (1970-07-01)
N Jayasree et al.
Journal - Association of Official Analytical Chemists, 70(4), 762-763 (1987-07-01)
Three simple titrimetric methods have been developed to determine iodine-bromine numbers of some edible oils, such as coconut, gingelly, groundnut, mustard, olive, palm olein, and sunflower, using 3 N-chloroimides. The 3 N-chloroimides are N-chlorophthalimide, N-chlorosuccinimide, and N-chlorosaccharin, all of which
Kevin I Booker-Milburn et al.
Organic letters, 5(18), 3313-3315 (2003-08-29)
[reaction: see text] N-Chlorosaccharin has been shown to undergo electrophilic Ritter-type reactions with alkenes in acetonitrile. The resulting labile beta-chloro sulfonylamidines can be ring-opened and cyclized to imidazolines. Overall this provides a one pot method for the electrophilic diamination of
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