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[ CAS No. 128-44-9 ] {[proInfo.proName]}

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Chemical Structure| 128-44-9
Chemical Structure| 128-44-9
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Product Details of [ 128-44-9 ]

CAS No. :128-44-9 MDL No. :MFCD00013092
Formula : C7H4NNaO3S Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 205.17 Pubchem ID :-
Synonyms :
Chemical Name :1,2-Benzothiazol-3(2H)-one 1,1-dioxide sodium salt

Safety of [ 128-44-9 ]

Signal Word:Danger Class:6.1
Precautionary Statements:P261-P280-P305+P351+P338 UN#:2811
Hazard Statements:H302-H312-H315-H319-H332-H335-H350 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 128-44-9 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 128-44-9 ]

[ 128-44-9 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 58929-72-9 ]
  • [ 128-44-9 ]
  • 1,1,1',1'-tetraoxo-2,2'-(4-oxa-heptanediyl)-bis-1λ6-benz[<i>d</i>]isothiazol-3-one [ No CAS ]
  • 2
  • [ 2895-21-8 ]
  • [ 128-44-9 ]
  • [ 77696-96-9 ]
  • 3
  • [ 128-44-9 ]
  • [ 156001-49-9 ]
  • [ 1026505-61-2 ]
  • 4
  • [ 72287-26-4 ]
  • [ 128-44-9 ]
  • [ 1428786-60-0 ]
YieldReaction ConditionsOperation in experiment
83% In ethanol; chloroform; at 20℃; for 3h; 2.3 [PdCl(sac)(kappa2-dppf)] (2) A warm ethanol (10 cm3) solution of sodium saccharinate (0.112 g, 0.55 mmol) was added to a chloroform (20 cm3) solution of [PdCl2(kappa2-dppf)] (0.20 g, 0.27 mmol). Following a similar procedure to above, [PdCl(sac)(kappa2-dppf)] (2) was isolated as a red-brown crystalline solid in 83percent yield. 1H NMR: delta 8.31-7.01 (m, 24H, Ar), 4.32 (br, 4H, CH), 3.42 (br, 4H, CH); 31P{1H} NMR: delta 37.20 (d, JPP 12.7 Hz), 28.99 (d, JPP 12.7 Hz). IR nu/cm-1; IR(KBr) 3058w, 3051w, 2972w, 2918w, 1670s, 1586m, 1433m, 1294s, 1247s, 1155vs, 962m, 482s cm-1; Elemental Anal. Calc. for PdFeSNClP2O3C41H32: C, 56.06; H, 3.67; N, 1.59. Found: C, 56.26; H, 3.40; N, 1.70percent.
  • 5
  • [ 128-44-9 ]
  • [ 15366-32-2 ]
  • amino((2-ethoxy-2-oxoethyl)(methyl)amino)methaniminium 3-oxo-3H-benzo[d]isothiazol-2-ide 1,1-dioxide [ No CAS ]
YieldReaction ConditionsOperation in experiment
96% In ethanol; at 50℃; for 4h; To the solution of CEE hydrochloride 22 (1 .0 mmol, 195 mg) in EtCH (15 mL)equimolar quantity of sweetener salt (potassium 6-methyl-4-oxo-4H-1 ,2,3-oxathiazin-3-ide2,2-dioxide 0.201 g for 20a and sodium benzo[d]isothiazol-3-olate 1,1-dioxide hydrate 0.205g for 20b) was added and the mixture was then stirred for 4h at the 50 C. Sodium or potassium chloride, formed during the reaction, was separated by filtration through the 22 micron membrane filter and the filtrate was taken to dryness. Diethyl ether was added to the products and after it was evaporated, products 23a and 23b were isolated as white solids in quantitative yields.
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