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Chemical Structure| 60851-41-4 Chemical Structure| 60851-41-4

Structure of 60851-41-4

Chemical Structure| 60851-41-4

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Product Details of [ 60851-41-4 ]

CAS No. :60851-41-4
Formula : C42H68O11
M.W : 748.98
SMILES Code : O=C1[C@]2(O[C@@]3(O[C@]([C@H](C([C@H]([C@H]([C@H](C)[C@@]4(O[C@@]([C@H](C(O)=O)CC)(CC[C@@H]4C)[H])[H])O)C)=O)CC)([C@@H](C)C[C@H]3C)[H])C=C1)O[C@@](C)(CC2)[C@@]5(O[C@@H](C)[C@](CC)(O)CC5)[H]
MDL No. :N/A

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Application In Synthesis of [ 60851-41-4 ]

* 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 [ 60851-41-4 ]

[ 60851-41-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 321574-29-2 ]
  • [ 60851-41-4 ]
  • salinomycin-20-ketoxime-O-4'-trifluoromethylbenzyl ether [ No CAS ]
YieldReaction ConditionsOperation in experiment
52 mg With sodium acetate; In methanol; at 20℃; for 12h; C20-oxanamycin (100 mg, 0.134 mmol) was dissolved in 2 mL of methanol followed by sodium acetate (22 mg,0.268 mmol) and O- (4-trifluoromethylbenzyl) hydroxylamine hydrochloride (61 mg, 0.268 mmol) were added and the mixture was stirred at room temperature for 12 h. The reaction mixture was pouredInto the water, filtered to give a white precipitate. After column chromatography (mobile phase: petroleum ether: ethyl acetate = 6: 1), a white solid52mg.
 

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