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Chemical Structure| 16312-79-1 Chemical Structure| 16312-79-1

Structure of 16312-79-1

Chemical Structure| 16312-79-1

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Product Details of [ 16312-79-1 ]

CAS No. :16312-79-1
Formula : C3H5N3O2
M.W : 115.09
SMILES Code : O=C(N1C)NNC1=O
MDL No. :MFCD00005227

Safety of [ 16312-79-1 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 16312-79-1 ]

* 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 [ 16312-79-1 ]

[ 16312-79-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 16312-79-1 ]
  • [ 14752-66-0 ]
  • 1-((4-chlorophenyl)sulfonyl)-4-methyl-1,2,4-triazolidine-3,5-dione [ No CAS ]
YieldReaction ConditionsOperation in experiment
93% With laccase from Trametes versicolor; In aq. phosphate buffer; at 25℃; for 2.5h;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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