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Chemical Structure| 16717-64-9 Chemical Structure| 16717-64-9

Structure of 16717-64-9

Chemical Structure| 16717-64-9

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Product Details of [ 16717-64-9 ]

CAS No. :16717-64-9
Formula : C8H7N3
M.W : 145.16
SMILES Code : C=C(C1=CC=CC=C1)N=[N+]=[N-]

Safety of [ 16717-64-9 ]

Application In Synthesis of [ 16717-64-9 ]

* 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 [ 16717-64-9 ]

[ 16717-64-9 ] Synthesis Path-Downstream   1~7

  • 2
  • [ 16717-64-9 ]
  • [ 114046-25-2 ]
  • 4-(6-methoxy-4-phenylquinolin-2-yl)benzonitrile [ No CAS ]
  • 3
  • [ 16717-64-9 ]
  • [ 302348-51-2 ]
  • 2-(4-((1-azido-2-fluoro-1-phenylethoxy)methyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane [ No CAS ]
  • 4
  • [ 16717-64-9 ]
  • [ 302348-51-2 ]
  • 2-(4-((1-azido-2-bromo-1-phenylethoxy)methyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolane [ No CAS ]
  • 5
  • [ 16717-64-9 ]
  • [ 7194-78-7 ]
  • (Z)-3-amino-1-(3-bromophenyl)-3-phenylprop-2-en-1-one [ No CAS ]
  • 6
  • [ 16717-64-9 ]
  • [ 79477-87-5 ]
  • (Z)-3-amino-1-(3-fluorophenyl)-3-phenylprop-2-en-1-one [ No CAS ]
  • 7
  • [ 16717-64-9 ]
  • [ 14752-66-0 ]
  • (Z)-2-(4-chlorophenylsulfonyl)-1-phenylethenamine [ No CAS ]
YieldReaction ConditionsOperation in experiment
82% With ammonium iodide; In tetrahydrofuran; dimethyl sulfoxide; at 20℃; for 1.5h;Electrolysis; General procedure: An undivided cell was equipped with a graphite plate anode (3 cm2) and a stainless steel plate cathode (3 cm2) and connected to a DC regulated power supply. The solution of vinyl azide 1 (1 mmol), sodium sulfinate 2 (1.5 mmol) and supporting electrolyte NH4I (3 mmol) in 20 mL of DMSO-THF (1:1) was electrolyzed using constant current conditions (I = 60 mA, j = 20 mA/cm2 at room temperature, τ = 90 min) under magnetic stirring. After that the reaction mixture was diluted with 0.3 M solution of Na2S2O3 (50 mL) and washed with EA (5×10 mL), which was used for the washing of electrodes after the reaction. Combined organic layer was washed with 1 M solution of Na2S2O3 (10 mL), water (10 mL) and brine (10mL), dried over Na2SO4, and concentrated under reduced pressure. The desired products 3a-3k were isolated by chromatography with elution using PE-EA in a gradient of the latter from 5 to 50 vol%. In all eluents 2% of NEt3 was also added in order to prevent the products from hydrolysis.
52% With eosin Y disodium salt; nitrobenzene; In ethanol; at 20℃; for 14h;Inert atmosphere; Irradiation; General procedure: The solution of vinyl azides 1 (1 mmol), sodium sulfinate 2 (1.5mmol), eosin Y disodium salt (0.001 mmol, 7 mg), and nitrobenzene (1 mmol, 123 mg) in 4 mL of EtOH was irradiated with green LEDs for 14 hours (24 hours in the case of 3f) at room temperature under magnetic stirring. Then, EtOH was removed under reduced pressure. The residue was diluted with 50 mL of EA and washed with water (2×10 mL) and brine (2×10 mL). Combined water layer was washed with EA (2×10 mL). Combined organic layer was dried over Na2SO4 and concentrated under reduced pressure. The desired products 3a-3j were isolated by chromatography with elution using PE-EA in a gradient of the latter from 5 to 50 vol%. In all eluents 2% of NEt3 was also added in order to prevent hydrolysis of the products.
 

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