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Chemical Structure| 924868-97-3 Chemical Structure| 924868-97-3

Structure of 924868-97-3

Chemical Structure| 924868-97-3

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Product Details of [ 924868-97-3 ]

CAS No. :924868-97-3
Formula : C9H8ClN3
M.W : 193.63
SMILES Code : ClCC1=CN(C2=CC=CC=C2)N=N1
MDL No. :MFCD08444000

Safety of [ 924868-97-3 ]

Application In Synthesis of [ 924868-97-3 ]

* 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 [ 924868-97-3 ]

[ 924868-97-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 103755-58-4 ]
  • [ 924868-97-3 ]
YieldReaction ConditionsOperation in experiment
With thionyl chloride; In dichloromethane;Reflux; (l-Phenyl-lH-[l,2,3]triazol-4-yl)-methanol (700 mg) was treated with thionyl chloride (2 mL) in dichloromethane (10 mL). The mixture was stirred and heated under reflux to form a solution. The excess reagent and solvent were removed under vacuum and the residue dissolved in dichloromethane (50 mL). The dichloromethane solution was passed through a pad of silica which was further washed with dichloromethane followed by diethyl ether. The eluants were combined and concentrated to give the sub-titled compound as a solid (600 mg).1H NMR (400 MHz, CDCl3) 5 8.00 (IH, s), 7.73 - 7.68 (2H, m), 7.54 - 7.48 (2H, m), 7.47 - 7.41 (IH, m), 4.77 (2H, s).
With thionyl chloride; In dichloromethane;Reflux; Example 12: (R)-3-(l-Phenyl-cycloheptanecarbonyloxy)-l-(l-phenyl-lH- [1, 2,3]triazol-4-ylm ethyl)- l-azonia-bicyclo[2.2.2]octane chloridea) 4-Chloromethyl- 1 -phenyl- lH-[ 1 ,2,3]triazole (1 -Phenyl- IH-[1, 2, 3]triazol-4-yl)-methanol (700 mg) was treated with thionyl chloride (2 mL) in dichloromethane (10 mL). The mixture was stirred and heated under reflux to form a solution. The excess reagent and solvent were removed and the residue dissolved in dichloromethane (50 mL) and passed down a plug of silica gel. The silica was washed with <n="53"/>dichloromethane followed by ether and the eluants combined and concentrated to afford the sub-titled compound as a crystalline solid (600 mg).1H NMR (399.826 MHz, CDCl3) delta 8.00 (s, IH), 7.73 - 7.68 (m, 2H), 7.54 - 7.48 (m, 2H), 7.47 - 7.41 (m, IH), 4.77 (s, 2H).
  • 2
  • [ 39998-25-9 ]
  • [ 924868-97-3 ]
  • methyl 2-[1-[(1-phenyltriazol-4-yl)methyl]pyridin-1-ium-3-yl]acetate [ No CAS ]
YieldReaction ConditionsOperation in experiment
In N,N-dimethyl-formamide; at 115℃; for 2h; Methyl-3 -pyridylacetate (60 mg, 0.39 mmoL) and 4-chloromethy 1- 1 -phenyl- 1H- 1,2,3 - triazole (100 mg, 0.39 mmol) were dissolved in 2 DMF. The reaction mixture was stirred at 1 15 C for 2 h. Solvent was removed in vacuum. The dry residue was dissolved in 4 mL H20 and purified by HPLC prep to give to give 233 mg of desired product as white solid containing some NH4COO. (0431) HPLC method C-18 column: (0432) 0 min: 95% 25 mM NH4COO in H20, 5% 25 mM NH4COO in CH3CN / H20 (80:20); (0433) 0-40 min: 0% 25 mM NH4COO in H20, 100% 25 mM NH4COO in CH3CN / H20 (80:20); ppm 3.65 (s, 3 H) 4.08 (s, 2 H) 6.00 - 6.11 (m, 2 H) 7.49 - 7.58 (m, 1 H) 7.59 - 7.69 (m, 2 H) 7.84 - 7.92 (m, 2 H) 8.16 - 8.27 (m, 1 H) 8.36 (s, 4 H) 8.57 - 8.66 (m, 1 H) 9.00 - 9.08 (m, 2 H) 9.15 - 9.21 (m, 1 H). (0434) HPLC-MS (m/z) [M]+ calcd 309.13515 found 309.2
 

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