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Chemical Structure| 3366-65-2 Chemical Structure| 3366-65-2

Structure of 3366-65-2

Chemical Structure| 3366-65-2

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Product Details of [ 3366-65-2 ]

CAS No. :3366-65-2
Formula : C14H11N
M.W : 193.24
SMILES Code : NC1=CC=C2C(C=CC3=C2C=CC=C3)=C1
MDL No. :MFCD00032956

Safety of [ 3366-65-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501

Application In Synthesis of [ 3366-65-2 ]

* 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 [ 3366-65-2 ]

[ 3366-65-2 ] Synthesis Path-Downstream   1~4

  • 1
  • [ 3366-65-2 ]
  • [ 62162-97-4 ]
  • 2
  • [ 62162-97-4 ]
  • [ 3366-65-2 ]
YieldReaction ConditionsOperation in experiment
69% With ammonium sulfate; bis[tris(2-methylphenyl)phosphine]palladium; (R)-1-[(SP)-2-(dicyclohexylphosphino)ferrocenyl]ethyldi-tert-butylphosphine; sodium t-butanolate; In 1,4-dioxane; for 5h;Inert atmosphere; Reflux; Under argon atmosphere, a mixture of 18 <strong>[62162-97-4]2-bromophenanthrene</strong> (17.5 g, 68.0 mmol), 19 bis[tris(2-methylphenyl)phosphine]palladium (97 mg, 014 mmol), 20 (R)-1-[(SP)-2-(dicyclohexylphosphino)ferrocenyl]ethyldi-tert-butylphosphine (75 mg, 014 mmol), 21 ammonium sulfate (13.5 g, 102 mmol), 22 sodium t-butoxide (29.4 g, 306 mmol), and 23 dioxane (340 mL) was refluxed under heating for 5 h. After cooling to room temperature and adding 24 water, the reaction liquid was extracted with ethyl acetate. The organic layer was washed with water, dried over magnesium sulfate, and then concentrated. The obtained residue was purified by silica gel column chromatography to obtain 25 phenanthrene-2-amine (9.53 g, 69percent yield).
  • 3
  • [ 62162-97-4 ]
  • [ 3366-65-2 ]
  • C28H19N [ No CAS ]
YieldReaction ConditionsOperation in experiment
70% With tris-(dibenzylideneacetone)dipalladium(0); sodium t-butanolate; tri tert-butylphosphoniumtetrafluoroborate; In toluene; for 7.5h;Inert atmosphere; Reflux; Under argon atmosphere, a mixture of phenanthrene-2-amine (9.03 g, 46.7 mmol), <strong>[62162-97-4]2-bromophenanthrene</strong> (12.0 g, 46.7 mmol), tris(dibenzylideneacetone)dipalladium (0) (0.85 g, 0.93 mmol), tri-tert-butylphosphine tetrafluoroborate (1.09 g, 3.74 mmol), sodium t-butoxide (6.29 g, 65.4 mmol), and toluene (250 mL) was refluxed under heating for 7.5 h. After cooling to room temperature, the reaction liquid was concentrated. Methanol was added and the precipitated solid was collected by filtration. The obtained solid was purified by silica gel column chromatography to obtain the compound A5 (12.1 g, 70percent yield).
  • 4
  • [ 1256544-32-7 ]
  • [ 3366-65-2 ]
  • C30H19NO [ No CAS ]
YieldReaction ConditionsOperation in experiment
17 g With palladium diacetate; triphenylphosphine; sodium t-butanolate; In toluene; at 80℃; for 8h;Inert atmosphere; Under argon atmosphere, 9.66g (50mmol) 2- phenanthryl amine, 14.86g (50mmol) 9- bromo - two-benzo [2,1-B] furan, 9.60g (100mmol) of tert-butanol Sodium was dissolved in 500 ml of dehydrated toluene, and 0.23 g(1 mmol) of palladium acetate and 0.20 g (1 mmol) of triphenylphosphinewere added under stirring, and the mixture wasreacted at 80 C for 8 hours.After cooling, it was filtered through a Celite/silica gel, and the filtrate was evaporated to remove organic solvent. The residue obtained was crystallized from toluene and dried to give 17.0 g(41.5 mmol) of Compound N4.
 

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