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Chemical Structure| 104224-50-2 Chemical Structure| 104224-50-2

Structure of 104224-50-2

Chemical Structure| 104224-50-2

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Product Details of [ 104224-50-2 ]

CAS No. :104224-50-2
Formula : C15H19ClO
M.W : 250.76
SMILES Code : O=C(Cl)C1=CC=C2C(C)(C)CCC(C)(C)C2=C1

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Application In Synthesis of [ 104224-50-2 ]

* 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 [ 104224-50-2 ]

[ 104224-50-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 26807-73-8 ]
  • [ 104224-50-2 ]
  • 5,5,8,8-tetramethyl-5,6,7,8-tetrahydro-naphthalene-2-carboxylic acid (1-benzyl-1<i>H</i>-indol-5-yl)-amide [ No CAS ]
  • 2
  • [ 35418-07-6 ]
  • [ 104224-50-2 ]
  • [ 1020281-06-4 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In dichloromethane; at 0 - 20℃; for 16.5h; Example 13: Propionic acid ester analogue (18) of Am-580 [Show Image] A solution of the compound 17 (39 mg, 0.168 mmol) in benzene (2.5 ml) was added with thionyl chloride (122 mu 1, 1.67 mmol) and DMF (1 drop), and the mixture was refluxed by heating for 1 hour. Volatile substances were evaporated, then the residue was added with benzene (3 ml), the solvent was evaporated again, and the residue was dried under reduced pressure. A solution of this residue in dichloromethane (1 ml) was cooled on ice, and added with a solution of <strong>[35418-07-6]methyl 3-(4-aminophenyl)propionate</strong> (36 mg, 0.201 mmol) and triethylamine (117 mul, 0.841 mmol) in dichloromethane (2 ml), and the mixture was stirred at 0C for 30 minutes, and at room temperature for further 16 hours. The reaction mixture was added with saturated aqueous sodium hydrogencarbonate, and extracted with ethyl acetate. The organic layer was washed with water, and dried over anhydrous sodium sulfate, and then the solvent was evaporated. The residue was purified by silica gel column chromatography (eluted with chloroform), and the residue was recrystallized to obtain the title compound 18 (55 mg, 83%) together with the recovered compound 17 (6 mg, 15%). Compound 18: colorless needles, melting point: 118.5-119.5C (dichloromethane-hexane) MS (m/z): 393 (M+, 15). 249 (4), 215 (100), 172 (5), 157 (10), 91 (6), 43 (9) IR (KBr) cm1: 1731, 1638 1H-NMR (CDCl3) delta:1.29 (6H, s), 1.30 (6H, s), 1.70 (4H, s), 2.61 (2H, t, J=8 Hz), 2.92 (2H, t, J=8 Hz), 3.66 (3H, s), 7.17 (2H, A2B2, ,J=8.5 Hz), 7.36 (1H, d, J=8 Hz), 7.55 (1H, dd, J=8, 2 Hz), 7.56 (2H, A2B2, J=8.5 Hz), 7.86 (1H, d, J=2 Hz), 7.99 (1H, br s, CONH)
With triethylamine; In dichloromethane; at 0 - 20℃; for 16.5h; Example 13; Propionic Acid Ester Analogue (18) of Am-580; A solution of the compound 17 (39 mg, 0.168 mmol) in benzene (2.5 ml) was added with thionyl chloride (122 mul, 1.67 mmol) and DMF (1 drop), and the mixture was refluxed by heating for 1 hour. Volatile substances were evaporated, then the residue was added with benzene (3 ml), the solvent was evaporated again, and the residue was dried under reduced pressure. A solution of this residue in dichloromethane (1 ml) was cooled on ice, and added with a solution of <strong>[35418-07-6]methyl 3-(4-aminophenyl)propionate</strong> (36 mg, 0.201 mmol) and triethylamine (117 mul, 0.841 mmol) in dichloromethane (2 ml), and the mixture was stirred at 0 C. for 30 minutes, and at room temperature for further 16 hours. The reaction mixture was added with saturated aqueous sodium hydrogencarbonate, and extracted with ethyl acetate. The organic layer was washed with water, and dried over anhydrous sodium sulfate, and then the solvent was evaporated. The residue was purified by silica gel column chromatography (eluted with chloroform), and the residue was recrystallized to obtain the title compound 18 (55 mg, 83%) together with the recovered compound 17 (6 mg, 15%).Compound 18: colorless needles, melting point: 118.5-119.5 C. (dichloromethane-hexane)MS (m/z): 393 (M+, 15), 249 (4), 215 (100), 172 (5), 157 (10), 91 (6), 43 (9)IR (KBr) cm-1: 1731, 16381H-NMR (CDCl3) delta: 1.29 (6H, s), 1.30 (6H, s), 1.70 (4H, s), 2.61 (2H, t, J=8 Hz), 2.92 (2H, t, J=8 Hz), 3.66 (3H, s), 7.17 (2H, A2B2, J=8.5 Hz), 7.36 (1H, d, J=8 Hz), 7.55 (1H, dd, J=8, 2 Hz), 7.56 (2H, A2B2, J=8.5 Hz), 7.86 (1H, d, J=2 Hz), 7.99 (1H, br s, CONH)
 

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