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Chemical Structure| 24897-34-5 Chemical Structure| 24897-34-5

Structure of 24897-34-5

Chemical Structure| 24897-34-5

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Product Details of [ 24897-34-5 ]

CAS No. :24897-34-5
Formula : C6H10O
M.W : 98.14
SMILES Code : C=CC(C1CC1)O
MDL No. :MFCD01860564

Safety of [ 24897-34-5 ]

GHS Pictogram:
Signal Word:Danger
Hazard Statements:H225-H315-H319-H335
Precautionary Statements:P210-P240-P241-P242-P243-P261-P264-P271-P280-P302+P352-P303+P361+P353-P304+P340-P305+P351+P338-P312-P332+P313-P337+P313-P362-P370+P378-P403+P233-P403+P235-P405-P501
Class:3
UN#:1993
Packing Group:

Application In Synthesis of [ 24897-34-5 ]

* 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 [ 24897-34-5 ]

[ 24897-34-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 221044-05-9 ]
  • [ 24897-34-5 ]
  • 1-cyclopropyl-3-(1-(pyrimidin-2-yl)-1H-indol-2-yl)propan-1-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
85% With silver hexafluoroantimonate; at 20℃; for 24h; To the polyethylene glycol-400 catalytic system obtained in Example 11 was added 1 mmol of N-pyrimidine indole and 2 mmol of 1-cyclopropylpropen-1-ol,Stir at room temperature for 24 hours, monitor the progress of the reaction by TLC,After the reaction is complete, extract with ether three times,The obtained polyethylene glycol-400 catalytic system is reused,Put into the next experiment, combine the ether solution and concentrate, and separate it by column chromatography,248 mg of light yellow oily liquid was obtained with a yield of 85%,The structural formula of the obtained product is as follows. The obtained polyethylene glycol-400 catalytic system is reused and put into the next experiment:
82% With silver hexafluoroantimonate; dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer; In water; at 80℃; for 12h;Schlenk technique; Green chemistry; General procedure: Heterocycles 1 (0.2mmol, 1.0 equiv), allylic alcohols 2 (0.4 mmol, 2.0 equiv), [Cp*RhCl2]2 (2.5mol %), AgSbF6 (0.02mmol, 10mol %) and H2O (2mL) were charged into a Schlenk tube under air. The reaction mixture was stirred for 12hat 80C. After the reaction was complete, the mixture was extracted with CH2Cl2 three times. The combined organic layer was dried with anhydrous Na2SO4 and evaporated in vacuum. The crude product was purified by flash chromatography on silica gel using hexane/ethyl acetate as the eluent to give the pure product 3.
 

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