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[ CAS No. 52188-11-1 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 52188-11-1
Chemical Structure| 52188-11-1
Structure of 52188-11-1 * Storage: {[proInfo.prStorage]}
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Product Details of [ 52188-11-1 ]

CAS No. :52188-11-1 MDL No. :MFCD00688358
Formula : C9H7NO5S Boiling Point : -
Linear Structure Formula :- InChI Key :MQAZHTHFEBUHCD-UHFFFAOYSA-N
M.W : 241.22 Pubchem ID :818753
Synonyms :

Safety of [ 52188-11-1 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501 UN#:N/A
Hazard Statements:H302-H315-H319-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 52188-11-1 ]

* 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 [ 52188-11-1 ]

[ 52188-11-1 ] Synthesis Path-Downstream   1~6

  • 1
  • [ 52188-11-1 ]
  • [ 42854-62-6 ]
  • [ 474900-01-1 ]
  • 2
  • [ 52188-11-1 ]
  • [ 1738-76-7 ]
  • [ 474900-02-2 ]
  • 3
  • [ 926224-90-0 ]
  • [ 52188-11-1 ]
  • [ 1221971-28-3 ]
YieldReaction ConditionsOperation in experiment
75% With tributyl-amine; 2-chloro-1-methyl-pyridinium iodide In dichloromethane for 1h; Reflux;
  • 4
  • [ 52188-11-1 ]
  • [ 538-51-2 ]
  • trans-2-(-2-oxo-1,4-diphenylazetidin-3-yl)benzo[d]isothiazol-3(2H)-one-1,1-dioxide [ No CAS ]
YieldReaction ConditionsOperation in experiment
86% With 2-chloro-1-methyl-pyridinium iodide; triethylamine In dichloromethane at 100℃; for 0.166667h; Microwave irradiation; diastereoselective reaction; 3 General procedure B, cycloaddition General procedure: A microwave vial wascharged with dichloromethane the appropriate imine (1.0 equiv),saccharinyl acetic acid (1.0 equiv), Mukaiyama’s salt (1.05 equiv)and triethylamine (2 equiv). The mixture was heated for 10 minin the microwave at 100 C. After the reaction, the mixture wasconcentrated in vacuo and puried on a preparative LCMS. WatersX-Bridge 30 mm 150 mm C18 column; gradient, CH3CN:H2O(0.1% TFA). Fractions containing the product were automaticallycollected based on observed mass and UV-signal after which theywere lyophilized to obtain the pure products.
  • 5
  • [ 22179-78-8 ]
  • [ 52188-11-1 ]
  • 2‐[3‐(4‐fluorophenyl)‐1,2,4‐oxadiazol‐5‐yl]methyl}benzo[d]isothiazol‐3(2H)‐one 1,1‐dioxide [ No CAS ]
YieldReaction ConditionsOperation in experiment
52% Stage #1: 4-fluoro-N'-hydroxybenzimidamide; 2-(1,1-dioxido-3-oxobenzo[d]isothiazol-2(3H)-yl)acetic acid With triethylamine In ethyl acetate for 0.5h; Inert atmosphere; Stage #2: With 1-propanephosphonic acid cyclic anhydride In ethyl acetate Inert atmosphere;
  • 6
  • [ 52188-11-1 ]
  • [ 19227-14-6 ]
  • 2‐[3‐(4‐bromophenyl)‐1,2,4‐oxadiazol‐5‐yl]methyl}benzo[d]isothiazol‐3(2H)‐one 1,1‐dioxide [ No CAS ]
YieldReaction ConditionsOperation in experiment
56% Stage #1: 2-(1,1-dioxido-3-oxobenzo[d]isothiazol-2(3H)-yl)acetic acid; 4-bromo-N'-hydroxybenzimidamide With triethylamine In ethyl acetate for 0.5h; Inert atmosphere; Stage #2: With 1-propanephosphonic acid cyclic anhydride In ethyl acetate Inert atmosphere;
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