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Chemical Structure| 38945-01-6 Chemical Structure| 38945-01-6

Structure of 38945-01-6

Chemical Structure| 38945-01-6

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Product Details of [ 38945-01-6 ]

CAS No. :38945-01-6
Formula : C4H3NaO2S2
M.W : 170.19
SMILES Code : O=S(C1=CC=CS1)[O-].[Na+]
MDL No. :MFCD11656003
InChI Key :RRLLXOFIOPVYOP-UHFFFAOYSA-M
Pubchem ID :23674657

Safety of [ 38945-01-6 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
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

Application In Synthesis of [ 38945-01-6 ]

* 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 [ 38945-01-6 ]

[ 38945-01-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 110-05-4 ]
  • [ 38945-01-6 ]
  • [ 38695-60-2 ]
YieldReaction ConditionsOperation in experiment
89% In water; at 100℃; for 10h;Sealed tube; In the reflux reactor,Followed by adding 0.5mmlSodium 2-thienylsulfinate,1 mmol di-tert-butyl peroxide,2.5mL water; magnetic stirring, heat sealed at 100 for 10 hours;After stopping heating, cool to room temperature and then use ethyl acetateThe reaction mixture was extracted three times; the ethyl acetate was removed under reduced pressure to obtain the target 2-thienylmethylsulfone.The structure of the resulting product was confirmed by GC-MS, 1H NMR, 13C NMR.The yield of 2-thienylmethylsulfone was 89%
89% With water; at 110℃; for 12h;Sealed tube; Green chemistry; General procedure: Sodium benzenesulfinate (0.5 mmol), 2-(tert-butylperoxy)-2-methylpropane (1 mmol), and H2O (2.5 mL) were added into a 10 mL sealed tube successively. Then, the reaction was carried out at 110 C under magnetic stirring for 12 h. After the reaction was finished, the reaction mixture was extracted with ethyl acetate for three times (5 mL × 3). The obtained organic layer was dried with anhydrous MgSO4. The solvent was removed under vacuum, and the obtained crude product was purified by silica gel column chromatography with petroleum ether/ethyl acetate (10:1) as eluent to afford the desired pure product.
  • 2
  • [ 38945-01-6 ]
  • [ 2905-56-8 ]
  • C16H17NO2S2 [ No CAS ]
 

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