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[ CAS No. 106510-95-6 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 106510-95-6
Chemical Structure| 106510-95-6
Structure of 106510-95-6 * Storage: {[proInfo.prStorage]}
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Product Details of [ 106510-95-6 ]

CAS No. :106510-95-6 MDL No. :MFCD05742386
Formula : C15H11NS Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 237.32 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 106510-95-6 ]

* 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 [ 106510-95-6 ]

[ 106510-95-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 1532-91-8 ]
  • [ 930-69-8 ]
  • [ 106510-95-6 ]
  • 2
  • [ 108-98-5 ]
  • [ 192182-56-2 ]
  • [ 106510-95-6 ]
YieldReaction ConditionsOperation in experiment
61% With tetra(n-butyl)ammonium hydroxide; oxygen; In ethanol; water; at 25℃; for 8h;Schlenk technique; Green chemistry; General procedure: An oven-dried Schlenk tuble equipped with a magnetic stirring bar was charged with MCM-41-1,10-Phen-CuSO4 (30 mg, 0.025 mmol), arylboronic acid (0.5 mmol), and thiol (0.75 mmol) (if solid). The tube was evacuated and filled with oxygen. Then EtOH (0.5 mL) was added by a syringe under a counter flow of oxygen. After stirring for 5 min, n-Bu4NOH (40% aq) (0.5 mL) was added by a syringe under a counter flow of oxygen. Next, thiol (0.75 mmol) (if liquid) was added by a syringe under a counter flow of oxygen. The resulting reaction mixture was stirred at 25 C for 8-24 h. The reaction mixture was then diluted with EtOAc (20 mL), and filtered. The MCM-41-1,10-Phen-CuSO4 complex was washed with distilled water (2×5 mL) and EtOH (3×5 mL), and reused in the next run. The filtrate was washed with water (2×5 mL) and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure and the residue was purified by flash column chromatography on silica gel.
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