Basic information Safety Supplier Related

N-CHLOROSACCHARIN

Basic information Safety Supplier Related

N-CHLOROSACCHARIN Basic information

Product Name:
N-CHLOROSACCHARIN
Synonyms:
  • 2-CHLORO-1,2-BENZISOTHIAZOL-3(2H)ONE 1,1-DIOXIDE
  • N-Chlorosaccharin,98%
  • N-CHLOROSACCHARIN
  • N-Chlorosaccharin 99%
  • 1,2-Benzisothiazol-3(2H)-one, 2-chloro-, 1,1-dioxide
  • 2-Chlorobenzo[d]isothiazol-3(2H)-one 1,1-dioxide
  • N-Chlorosaccharin
CAS:
14070-51-0
MF:
C7H4ClNO3S
MW:
217.63
Product Categories:
  • Building Blocks
  • Halogenated Heterocycles
  • Heterocyclic Building Blocks
  • Thiazoles
  • ThiazolesHeterocyclic Building Blocks
Mol File:
14070-51-0.mol
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N-CHLOROSACCHARIN Chemical Properties

Melting point:
148-152 °C (lit.)
Boiling point:
388.6±25.0 °C(Predicted)
Density 
1.77±0.1 g/cm3(Predicted)
storage temp. 
Sealed in dry,2-8°C
solubility 
soluble in Toluene
form 
powder to crystaline
pka
-24.37±0.20(Predicted)
color 
White to Almost white
InChI
InChI=1S/C7H4ClNO3S/c8-9-7(10)5-3-1-2-4-6(5)13(9,11)12/h1-4H
InChIKey
VKWMGUNWDFIWNW-UHFFFAOYSA-N
SMILES
S1(=O)(=O)C2=C(C=CC=C2)C(=O)N1Cl
CAS DataBase Reference
14070-51-0
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Safety Information

Hazard Codes 
Xn
Risk Statements 
20/21/22-40
Safety Statements 
22-26-36/37/39
WGK Germany 
3
HS Code 
29251100

MSDS

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N-CHLOROSACCHARIN Usage And Synthesis

Chemical Properties

White to off-white crystalline powder

Synthesis

81-07-2

14070-51-0

1. Saccharin (6.0 g) was dissolved in methanol (120 mL), stirred at room temperature, tert-butyl hypochlorite (5 mL) was added slowly, and the reaction was carried out for 5 min to obtain N-chlorophthaloylbenzimide intermediate 1a (6.0 g, 84% yield). 2. Intermediate 1a (3.0 g) was mixed with silver trifluoromethylsulfide (3.6 g) in acetonitrile (40 mL), and the reaction was stirred at room temperature for 10 min to obtain the target product N-chlorophthaloylbenzimide 1 (3.3 g, 86% yield). Note: The product 1 is a white solid at room temperature, easily soluble in organic solvents such as dichloromethane, chloroform, acetone and acetonitrile.

References

[1] Synlett, 2006, # 2, p. 194 - 200
[2] Angewandte Chemie, International Edition, 2014, vol. 53, # 35, p. 9316 - 9320,5
[3] Angewandte Chemie, 2014, vol. 126, # 35, p. 9470 - 9474,5
[4] Patent: CN104945294, 2016, B. Location in patent: Paragraph 0135; 0136; 0137; 0138
[5] Patent: CN104945298, 2016, B. Location in patent: Paragraph 0187; 0188; 0189; 0190

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