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[ CAS No. 15988-11-1 ] {[proInfo.proName]}

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Chemical Structure| 15988-11-1
Chemical Structure| 15988-11-1
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Product Details of [ 15988-11-1 ]

CAS No. :15988-11-1 MDL No. :MFCD00005226
Formula : C8H7N3O2 Boiling Point : -
Linear Structure Formula :- InChI Key :GOSUFRDROXZXLN-UHFFFAOYSA-N
M.W : 177.16 Pubchem ID :85229
Synonyms :

Safety of [ 15988-11-1 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P280-P305+P351+P338 UN#:N/A
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 15988-11-1 ]

* 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 [ 15988-11-1 ]

[ 15988-11-1 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 58386-20-2 ]
  • [ 15988-11-1 ]
  • [ 54051-18-2 ]
  • 2
  • [ 15988-11-1 ]
  • [ 14752-66-0 ]
  • 1-((4-chlorophenyl)sulfonyl)-4-phenyl-1,2,4-triazolidine-3,5-dione [ No CAS ]
YieldReaction ConditionsOperation in experiment
86% With laccase from Trametes versicolor; In aq. phosphate buffer; at 25℃; for 5h;pH 5.0;Green chemistry; Enzymatic reaction; General procedure: In a 25 ml round-bottom flask, PBS (pH = 5.0, c = 0.10 M, 10 ml) and urazole derivatives (1.0 mmol) were mixed together. Next, laccase enzyme (50 U, 57.5 mg) and arylsulfinic acid sodium salt (1.0 mmol) were added and the reaction mixture stirred under air at room temperature for 2-7 h. After completion of the reaction (checked by TLC), the precipitated solid was collected by filtration and washed several times with water. After drying, the products were characterized by IR, 1H NMR, 13C NMR and elemental analysis.
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