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Chemical Structure| 4703-22-4 Chemical Structure| 4703-22-4

Structure of 4703-22-4

Chemical Structure| 4703-22-4

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Product Details of [ 4703-22-4 ]

CAS No. :4703-22-4
Formula : C12H17NO2S
M.W : 239.33
SMILES Code : O=S(N1CCCCC1)(C2=CC=C(C)C=C2)=O
MDL No. :MFCD00159367
InChI Key :IGWGXOHABPCPHZ-UHFFFAOYSA-N
Pubchem ID :78431

Safety of [ 4703-22-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319
Precautionary Statements:P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313

Application In Synthesis of [ 4703-22-4 ]

* 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 [ 4703-22-4 ]

[ 4703-22-4 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 110-89-4 ]
  • [ 1153-45-3 ]
  • [ 100-02-7 ]
  • [ 4703-22-4 ]
  • [ 6574-15-8 ]
  • 2
  • [ 2905-56-8 ]
  • [ 98-59-9 ]
  • [ 4703-22-4 ]
YieldReaction ConditionsOperation in experiment
75.5% With alizarin yellow R; In acetonitrile; at 20℃; for 3h;Irradiation; N - benzylpiperidine (10 ml, 87.6 mg), p-toluenesulfonyl chloride (0.5 mmol, 142.9 mg), alizine R (0.75 mmol, 2.9 mg) and acetonitrile (5 μmol) were added to 2.0 mmol quartz tubes and reacted 3 hours at room temperature. By column chromatography gave the desired product 90.3 mg with a yield of 75.5%.
 

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