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[ CAS No. 238760-00-4 ] {[proInfo.proName]}

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Chemical Structure| 238760-00-4
Chemical Structure| 238760-00-4
Structure of 238760-00-4 * Storage: {[proInfo.prStorage]}
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Product Details of [ 238760-00-4 ]

CAS No. :238760-00-4 MDL No. :N/A
Formula : C18H20N2O Boiling Point : -
Linear Structure Formula :- InChI Key :YVXPCSYTPPMTHS-MRXNPFEDSA-N
M.W : 280.36 Pubchem ID :59767358
Synonyms :

Safety of [ 238760-00-4 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 238760-00-4 ]

* 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 [ 238760-00-4 ]

[ 238760-00-4 ] Synthesis Path-Downstream   1~8

  • 1
  • [ 117667-83-1 ]
  • [ 112245-13-3 ]
  • [ 238760-00-4 ]
YieldReaction ConditionsOperation in experiment
78% In dichloromethane at 50℃; for 16h; D Methyl-6-phenylpyridyl-2-imidate (0.200 g, 0.942 mmol) and (S)-tert-leucinol (0.122 g, 1.04 mmol) were dissolved in CH2CI2 (4 ml_). The reaction vessel was sealed and heated in a heating block (50 0C) for 16 hours and the reaction mixture was then cooled to ambient temperature. The reaction mixture was loaded onto the top of a Biotage cartridge (silica gel, 40S) and the product was eluted using a stepped gradient of 0 to 40% ethyl acetate in hexanes as the eluent. The product was obtained after evaporation of the eluent as a white solid (0.205 g, 78%).
  • 2
  • [ 98-80-6 ]
  • [ 238760-00-4 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1.1: tetrakis(triphenylphosphine) palladium(0) 2.1: <i>tert</i>-butyl alcohol / 2 h / 20 °C / Inert atmosphere 2.2: 16 h / 70 °C / Inert atmosphere
  • 3
  • [ 112245-13-3 ]
  • [ 157402-44-3 ]
  • [ 238760-00-4 ]
  • 4
  • [ 238760-00-4 ]
  • palladium dichloride [ No CAS ]
  • [(S)-4-(tert-butyl)-2-(6-phenylpyridin-2-yl)-4,5-dihydrooxazole]-palladium(II) chloride [ No CAS ]
YieldReaction ConditionsOperation in experiment
48% With sodium hydrogencarbonate In toluene for 16h; Inert atmosphere; Reflux;
  • 5
  • [ 34160-40-2 ]
  • [ 238760-00-4 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1.1: tetrakis(triphenylphosphine) palladium(0) 2.1: <i>tert</i>-butyl alcohol / 2 h / 20 °C / Inert atmosphere 2.2: 16 h / 70 °C / Inert atmosphere
  • 6
  • [ 1008-89-5 ]
  • [ 238760-00-4 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 2 steps 1.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0 - 20 °C / Schlenk technique; Inert atmosphere 1.2: 20 °C / Schlenk technique; Inert atmosphere 2.1: sodium methoxide / methanol / 20 °C / Schlenk technique; Inert atmosphere 2.2: 80 °C / Schlenk technique; Inert atmosphere
  • 7
  • [ 39065-47-9 ]
  • [ 112245-13-3 ]
  • [ 238760-00-4 ]
YieldReaction ConditionsOperation in experiment
Stage #1: 6-phenyl-pyridine-2-carbonitrile With sodium methoxide In methanol at 20℃; Schlenk technique; Inert atmosphere; Stage #2: L-tert-leucinol With toluene-4-sulfonic acid In toluene at 80℃; Schlenk technique; Inert atmosphere;
  • 8
  • [ 109-04-6 ]
  • [ 238760-00-4 ]
YieldReaction ConditionsOperation in experiment
Multi-step reaction with 3 steps 1.1: anhydrous sodium carbonate; tetrakis-(triphenylphosphine)-palladium / ethanol; toluene; lithium hydroxide monohydrate / 4 h / Schlenk technique; Inert atmosphere; Reflux 2.1: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0 - 20 °C / Schlenk technique; Inert atmosphere 2.2: 20 °C / Schlenk technique; Inert atmosphere 3.1: sodium methoxide / methanol / 20 °C / Schlenk technique; Inert atmosphere 3.2: 80 °C / Schlenk technique; Inert atmosphere
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[ 238760-00-4 ]

Chemical Structure| 2757082-75-8

A1353085[ 2757082-75-8 ]

(R)-4-(tert-Butyl)-2-(6-phenylpyridin-2-yl)-4,5-dihydrooxazole

Reason: Optical isomers