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Chemical Structure| 892408-42-3 Chemical Structure| 892408-42-3

Structure of 892408-42-3

Chemical Structure| 892408-42-3

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Product Details of [ 892408-42-3 ]

CAS No. :892408-42-3
Formula : C16H23NO5S
M.W : 341.42
SMILES Code : O=C(N1CC(COS(=O)(C2=CC=C(C)C=C2)=O)C1)OC(C)(C)C
MDL No. :MFCD09951817

Safety of [ 892408-42-3 ]

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 [ 892408-42-3 ]

* 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 [ 892408-42-3 ]

[ 892408-42-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 892408-42-3 ]
  • [ 253176-94-2 ]
YieldReaction ConditionsOperation in experiment
With lithium iodide; In acetone; at 35℃; for 16h; To a solution of 1.94 g of tert-butyl 3-[(tosyloxy)methyl]azetidin-1-carboxylate in 15.5 ml acetone were added 837 mg of lithium iodide and the reaction mixture was stirred for 16 hours at 35 C. After cooling, it was diluted with 200 ml ethyl acetate and the organic phase washed twice with 30 ml portions of water and once with 20 ml saturated sodium chloride solution. After drying over sodium sulphate and filtration, this was concentrated in vacuo. In this manner, 1.6 g of tert-butyl-3-(iodomethyl)azetidin-1-carboxylate were obtained, which was further reacted without purification.
  • 2
  • [ 892408-42-3 ]
  • [ 5930-94-9 ]
  • tert-butyl 3-((3-nitro-1H-pyrrol-1-yl)methyl)azetidine-1-carboxylate [ No CAS ]
 

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