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Chemical Structure| 135853-33-7 Chemical Structure| 135853-33-7

Structure of 135853-33-7

Chemical Structure| 135853-33-7

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Product Details of [ 135853-33-7 ]

CAS No. :135853-33-7
Formula : C13H10N4
M.W : 222.25
SMILES Code : C1(C2=NC=CC=C2)=NC(N3N=CC=C3)=CC=C1
MDL No. :MFCD28385939
InChI Key :VIMBMAKZWNNQGI-UHFFFAOYSA-N
Pubchem ID :12107912

Safety of [ 135853-33-7 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 135853-33-7 ]

* 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 [ 135853-33-7 ]

[ 135853-33-7 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 288-13-1 ]
  • [ 13040-77-2 ]
  • [ 135853-33-7 ]
YieldReaction ConditionsOperation in experiment
39% With potassium tert-butylate; In dimethyl sulfoxide; at 140℃; for 14h; Example 1 Synthesis of Bipyridine-Pyrazole Ligand tBuOK (2g) was added to a suspension of pyrazole (1 g) in dmso (80 mL) and stirred until a clear solution has formed. 6-chloro-2,2'-bipyridine (1g, from HetCat) was added slowly by portion and the mixture heated at 140 C for 14 hours. After cooling down to room temperature, water was added and the precipitate filtered and wash with water. The compound was further purified by silica gel chromatography column using Ethyl acetate/diethyl ether as eluent, leading to an off-white crystalline solid (450 mg, yield 39 %). Spectroscopic analysis are as reported in the literature ().
39% With potassium tert-butylate; at 140℃; for 14h; Example 1 : Synthesis of Bipyridine-Pyrazole Ligand tBuOK (2g) was added to a suspension of pyrazole (1 g) in dmso (80 mL) and stirred until a clear solution has formed. 6-chloro-2,2'-bipyridine (lg, from HetCat) was added slowly by portion and the mixture heated at 140 C for 14 hours. After cooling down to room temperature, water was added and the precipitate filtered and wash with water. The compound was further purified by silica gel chromatography column using Ethyl acetate/diethyl ether as eluent, leading to an off-white crystalline solid (450 mg, yield 39 %). Spectroscopic analysis are as reported in the literature (Inorg. Chem. 1991, 30, 3733).
 

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