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Chemical Structure| 28383-65-5 Chemical Structure| 28383-65-5

Structure of 28383-65-5

Chemical Structure| 28383-65-5

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Product Details of [ 28383-65-5 ]

CAS No. :28383-65-5
Formula : C11H10N2O3
M.W : 218.21
SMILES Code : O=C(OCC)C(C(C1=CC=CC=C1)=O)=[N+]=[N-]

Safety of [ 28383-65-5 ]

Application In Synthesis of [ 28383-65-5 ]

* 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 [ 28383-65-5 ]

[ 28383-65-5 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 13139-28-1 ]
  • [ 28383-65-5 ]
  • [ 182866-67-7 ]
  • 2
  • [ 55577-25-8 ]
  • [ 28383-65-5 ]
  • ethyl 3-methyl-6-phenyl-11H-benzo[a]carbazole-5-carboxylate [ No CAS ]
YieldReaction ConditionsOperation in experiment
76% With dichloro(pentamethylcyclopentadienyl)rhodium (III) dimer; copper diacetate; In acetonitrile; at 120℃; for 18h;Sealed tube; Was added to a 15 mL reaction tube compound 1f (0.55 mmol, 103.6 mg),Compound 2a (0.75 mmo 1,163.7 mg),bis(pentamethylcyclopentadienyl)dirhodium chloride (0.025 mmol, 15.5 mg)Copper acetate (0.05 mmol, 9 lmg) and acetonitrile (3 mL)The reaction tube is sealed in the presence of air,And then placed in a 120 C oil bath for 18 h.Add 10 mL of water to quench the reaction,Extracted with ethyl acetate (10 mL X), after which the organic phase was washed successively with water and saturated brine,Dried over anhydrous sodium sulfate. (Petroleum ether / ethyl acetate = 10/1) to give the product as a white solid 3-methyl-5-ethoxycarbonyl-6-phenyl-11H-benzo [a] carbazole 3f (144.5 mg, 76%).
  • 3
  • [ 28383-65-5 ]
  • [ 52562-19-3 ]
  • [ 142729-99-5 ]
YieldReaction ConditionsOperation in experiment
45% With dirhodium tetraacetate; copper diacetate; sodium carbonate; In 1,2-dichloro-ethane; at 100℃; for 16h;Sealed tube; General procedure: To a 25mL tube containing a magnetic stir bar, was added 2-vinylanilines 1 (0.2mmol), Rh2(OAc)4 (0.01mmol, 5mol%), Cu(OAc)2 (0.4mmol, 2.0 equiv), Na2CO3 (0.4mmol, 2.0 equiv), 1,2-DCE (2mL), and α-diazocarbonyl compounds 2 (0.4mmol, 2 equiv). The resulting mixture was stirred at 100C in air in sealed tube for 16h. After being cooled to room temperature, the reaction was monitored by TLC and the solvent was evaporated under reduced pressure. Purification was carried out by column chromatography using a mixture of ethyl acetate and petroleum ether (1:10 to 1:20) as eluent to obtain the desired product 3.
  • 4
  • [ 28383-65-5 ]
  • [ 128742-76-7 ]
  • methyl 3-(3-ethoxy-3-oxo-2-phenylpropanoyl)-1-methyl-1H-indole-5-carboxylate [ No CAS ]
  • 5
  • [ 28383-65-5 ]
  • [ 52562-19-3 ]
  • [ 4789-76-8 ]
YieldReaction ConditionsOperation in experiment
57% With trifluoroacetic acid; at 120℃; for 3h;Sealed tube; Dissolve 0.2 mmol of 2- (1-methylvinyl) aniline and 0.3 mmol of ethyl 2-diazo-3-oxo-3-phenylpropanoate in a pressure-resistant tube containing 1.6 mL of CF3COOH (equipped with Magnetic stirrer), fill the balloon with argon at least 3 times until the air is completely evacuated, close the pressure-resistant tube, and heat and stir at 120 C for 3h. After the reaction is complete, extract 3 times with 30mL of ethyl acetate and saturated sodium bicarbonate solution The organic phases were combined, dried over anhydrous MgSO4, concentrated, and separated by silica gel column chromatography to obtain 25.0 mg of a yellow oily compound with a yield of 57%.
 

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