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[ CAS No. 945681-56-1 ] {[proInfo.proName]}

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Chemical Structure| 945681-56-1
Chemical Structure| 945681-56-1
Structure of 945681-56-1 * Storage: {[proInfo.prStorage]}
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Product Details of [ 945681-56-1 ]

CAS No. :945681-56-1 MDL No. :
Formula : C26H14O12 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 518.38 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 945681-56-1 ]

* 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 [ 945681-56-1 ]

[ 945681-56-1 ] Synthesis Path-Downstream   1~7

  • 1
  • [ 883842-22-6 ]
  • [ 945681-56-1 ]
YieldReaction ConditionsOperation in experiment
78% With pyridine; potassium permanganate; water; sodium hydroxide at 80℃;
53% With potassium permanganate In pyridine; water for 24h; Heating;
  • 2
  • [ 945681-65-2 ]
  • [ 945681-56-1 ]
YieldReaction ConditionsOperation in experiment
60% With potassium permanganate In potassium hydroxide at 80℃; for 40h;
  • 3
  • [ 945681-56-1 ]
  • [ 64-17-5 ]
  • [ 947243-14-3 ]
YieldReaction ConditionsOperation in experiment
17% With sulfuric acid In ethanol for 144h; Heating;
  • 4
  • [ 945681-63-0 ]
  • [ 945681-56-1 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1: 96 percent / aq. KOH / methanol / 10 h / Heating 2: 60 percent / potassium permanganate / aq. KOH / 40 h / 80 °C
  • 5
  • [ 945681-56-1 ]
  • [ 1222074-43-2 ]
YieldReaction ConditionsOperation in experiment
With acetic anhydride at 165℃; for 24h;
  • 6
  • [ 55805-81-7 ]
  • [ 945681-56-1 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1.1: palladium diacetate; 2,2'-bis-(diphenylphosphino)-1,1'-binaphthyl; N-ethyl-N,N-diisopropylamine / 5,5-dimethyl-1,3-cyclohexadiene / 1 h / 20 °C / Inert atmosphere; Glovebox 1.2: 48 h / 120 - 140 °C / 22801.5 Torr / Autoclave 2.1: potassium hydroxide / tetrahydrofuran; water / Reflux
  • 7
  • [ CAS Unavailable ]
  • [ 945681-56-1 ]
YieldReaction ConditionsOperation in experiment
98% With potassium hydroxide In tetrahydrofuran; water Reflux; Carboxylic Acids 1b-8b by Hydrolysis of Esters 1a-8a: Typical Procedure B General procedure: To a THF solution (150 mL) of esters 1a-8a (5 mmol) was added H2O(50 mL), the mixture was stirred for 10 min at r.t., and then KOH (150mmol) was added and the mixture was heated to reflux until the reactionwas complete. The mixture was cooled to r.t. and concentrated to remove the THF. The residue was filtered and the filtrate was acidifiedto pH 3-5 with aq HCl (concd), resulting in the precipitation of alarge volume of solid. The solid was filtered off and the filter cake waswashed with water, and dried with a vacuum pump to give solid carboxylicacids 1b-8b
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