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Sigma-Aldrich

N-Chlorosaccharin

99%

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About This Item

Empirical Formula (Hill Notation):
C7H4ClNO3S
CAS Number:
Molecular Weight:
217.63
MDL number:
UNSPSC Code:
12352100
PubChem Substance ID:
NACRES:
NA.22

Assay

99%

mp

148-152 °C (lit.)

SMILES string

ClN1C(=O)c2ccccc2S1(=O)=O

InChI

1S/C7H4ClNO3S/c8-9-7(10)5-3-1-2-4-6(5)13(9,11)12/h1-4H

InChI key

VKWMGUNWDFIWNW-UHFFFAOYSA-N

Pictograms

Health hazardExclamation mark

Signal Word

Warning

Hazard Statements

Hazard Classifications

Acute Tox. 4 Oral - Carc. 2

Storage Class Code

11 - Combustible Solids

WGK

WGK 3

Flash Point(F)

Not applicable

Flash Point(C)

Not applicable

Personal Protective Equipment

dust mask type N95 (US), Eyeshields, Gloves

Certificates of Analysis (COA)

Search for Certificates of Analysis (COA) by entering the products Lot/Batch Number. Lot and Batch Numbers can be found on a product’s label following the words ‘Lot’ or ‘Batch’.

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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
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)
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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