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Chemical Structure| 153625-24-2 Chemical Structure| 153625-24-2

Structure of 153625-24-2

Chemical Structure| 153625-24-2

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Product Details of [ 153625-24-2 ]

CAS No. :153625-24-2
Formula : C13H18N2
M.W : 202.30
SMILES Code : N#CC1=CC(C(C)C)=C(N)C(C(C)C)=C1
MDL No. :MFCD24624073
InChI Key :HAALLPNOWFKZEH-UHFFFAOYSA-N
Pubchem ID :53637066

Safety of [ 153625-24-2 ]

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 [ 153625-24-2 ]

* 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 [ 153625-24-2 ]

[ 153625-24-2 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 544-92-3 ]
  • [ 80058-84-0 ]
  • [ 153625-24-2 ]
  • 2
  • copper(l) cyanide [ No CAS ]
  • [ 80058-84-0 ]
  • [ 153625-24-2 ]
YieldReaction ConditionsOperation in experiment
30% With copper(l) iodide; potassium iodide; N,N`-dimethylethylenediamine; In N,N-dimethyl-formamide; at 100℃; for 24h;Inert atmosphere; Into a 100-mL round-bottom flask purged with and maintained under nitrogen, was placed 4- bromo-2,6-diisopropylbenzenamine (commercial available, 5.1 g, 19.9 mmol), DMF (30 mL), CuCN (2.16 g, 23.9 mmol), CuI (380 mg, 2.00 mmol), KI (664 mg, 3.98 mmol), and DMEDA (2.0 mL). The resulting solution was stirred for 24 h at 100oC and then was diluted with 30 mL of water. The solution was extracted with 3x30 mL of ethyl acetate and the organic layers combined and concentrated under vacuum. The residue was applied onto a silica gel column and eluted with ethyl acetate/petroleum ether (1:30 to 1:20). This resulted in 1.2 g (30percent) of the title compound as a yellow solid. MS-ESI: 203.1 (M+1).
30% With copper(l) iodide; N,N-dimethylethylenediamine; potassium iodide; In N,N-dimethyl-formamide; at 100℃; for 24h;Inert atmosphere; Into a 100-mL round-bottom flask purged with and maintained under nitrogen, was placed <strong>[80058-84-0]4-bromo-2,6-diisopropylbenzenamine</strong> (commercial available, 5.1 g, 19.9 mmol), DMF (30 mL),CuCN (2.16 g, 23.9 mmol), Cul (380 mg, 2.00 mmol), KI (664 mg, 3.98 mmol), and DMEDA (2.0 mL). The resulting solution was stirred for 24 h at 100°C and then was diluted with 30 mL of water. The solution was extracted with 3x30 mL of ethyl acetate and the organic layers combined and concentrated under vacuum. The residue was applied onto a silica gel column and eluted withethyl acetate/petroleum ether (1:30 to 1:20). This resulted in 1.2 g (30percent) of the title compound as a yellow solid. MS-ESI: 203.1 (M+1).
  • 3
  • [ 557-21-1 ]
  • [ 80058-84-0 ]
  • [ 153625-24-2 ]
YieldReaction ConditionsOperation in experiment
80% With (1,1'-bis(diphenylphosphino)ferrocene)palladium(II) dichloride; potassium tert-butylate; In N,N-dimethyl-formamide; at 120℃; for 16h;Inert atmosphere; Into a 100-mL round-bottom flask purged with and maintained under nitrogen was placed a solution of <strong>[80058-84-0]4-bromo-2,6-diisopropylbenzenamine</strong> (5.1 g, 19.9 mmol) in DMF (30 mL). To the solution were added Zn(CN)2(2.80 g, 23.9 mmol), Pd(dppf)Cl2(732 mg, 1.00 mmol) and t-BuOK (3.36 g, 29.9 mmol). The resulting mixture was stirred for 16 h at 120°C and then was diluted with 30 mL of water. The solution was extracted with 3x30 mL of ethyl acetate and the combined organic layers were concentrated under vacuum. The residue was applied onto a silica gel column and eluted with a gradiente of ethyl acetate/petroleum ether (1 :30 to 1 :20). This resulted in 3.2 g (80percent) of the title compound as a yellow solid. MS-ESI: 203.1 (M+l).
2.460% With copper(l) iodide; triethylamine; In N,N-dimethyl-formamide; at 120℃; for 16h;Inert atmosphere; Into a 100-mL round-bottom flask purged with and maintained under nitrogen was placed a solution of <strong>[80058-84-0]4-bromo-2,6-diisopropylbenzenamine</strong> (commercially available, 5.1 g, 19.9 mmol) inDMF (30 mL). To the solution were added Zn(CN)2 (2.80 g, 23.9 mmol), Cul (380 mg, 2.00 mmol), and TEA (3.0 g, 29.9 mmol). The resulting solution was stirred for 16 h at 120°C and then was diluted with 30 mL of water. The solution was extracted with 3x30 mL of ethyl acetate and the combined organic layers were concentrated under vacuum. The residue was applied onto a silica gel column and eluted with ethyl acetate/petroleum ether (1:30 to 1:20). This resulted in 2.4 g (60percent) of the title compound as a yellow solid. MS-ESI: 203.1 (M+1).
 

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