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Chemical Structure| 16156-59-5 Chemical Structure| 16156-59-5
Chemical Structure| 16156-59-5

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Product Details of Phenyl Methanesulfonate

CAS No. :16156-59-5
Formula : C7H8O3S
M.W : 172.20
SMILES Code : CS(=O)(OC1=CC=CC=C1)=O
MDL No. :MFCD00095143
InChI Key :WXVUCMFEGJUVTN-UHFFFAOYSA-N
Pubchem ID :316170

Safety of Phenyl Methanesulfonate

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

Application In Synthesis of Phenyl Methanesulfonate

* 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 [ 16156-59-5 ]

[ 16156-59-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1006-68-4 ]
  • [ 16156-59-5 ]
  • [ 92-71-7 ]
YieldReaction ConditionsOperation in experiment
58% With bis(1,5-cyclooctadiene)nickel(0); 3,4-thiene-2,3-diylbis(dicyclohexylphosphine); caesium carbonate; In para-xylene; at 140℃; for 22h;Glovebox; Sealed tube; General procedure: Ni(COD)2, ligand (dcype or dcypt), base (Cs2CO3 or K3PO4), aryl electrophile (pivalates, mesylates or carbamates) and azole were weighed into in an oven dried 20 mL scintillation vial in the glove box. Xylene was added, the vial was sealed with a Teflon lined cap, taken out of the glove box and the reaction mixture was allowed to stir at the indicated temperature for the indicated time. The reaction mixture was cooled to room temperature and filtered through a 1.0 inch plug of silica gel, eluting with Et2O (125 mL). The filtrate was concentrated and chromatographed on a silica gel column to afford the product.
 

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