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Chemical Structure| 125973-55-9 Chemical Structure| 125973-55-9

Structure of 125973-55-9

Chemical Structure| 125973-55-9

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Product Details of [ 125973-55-9 ]

CAS No. :125973-55-9
Formula : C13H22O2Si2
M.W : 266.48
SMILES Code : O=C(O)C1=CC([Si](C)(C)C)=CC([Si](C)(C)C)=C1

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Application In Synthesis of [ 125973-55-9 ]

* 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 [ 125973-55-9 ]

[ 125973-55-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 35418-07-6 ]
  • [ 125973-55-9 ]
  • [ 1149744-44-4 ]
YieldReaction ConditionsOperation in experiment
88% Example 22: 4-(3,5-Bistrimethylsilanylbenzolyamino)phenylpropionic acid [Show Image] A solution of 3,5-bis(trimethylsilyl)benzoic acid (120 mg, 0.451 mmol) and cyanuric chloride (125 mg, 0.678 mmol) in acetone (4 ml) was cooled on ice, and added with triethylamine (251 mul, 1.80 mmol), and the mixture was stirred for 5 minutes. The mixture was further stirred at room temperature for 3.5 hours, and then added with <strong>[35418-07-6]methyl 3-(4-aminophenyl)propionate</strong> (121 mg, 0.676 mmol), and the mixture was further stirred for 16 hours. The reaction mixture was added with saturated aqueous sodium hydrogencarbonate, the mixture was extracted with ethyl acetate, the organic layer was treated in a conventional manner, and then the residue was separated by silica gel chromatography [eluted with benzene-ethyl acetate (14:1)], and recrystallized to obtain methyl 4-(3,5-bistrimethylsilanylbenzolyamino)phenylpropionate (169 mg, 88%) as colorless scales. Mp: 119-120.5C and 136-137C (dichloromethane-hexane) MS (m/z): 427 (M+, 25), 249 (100), 221 (9), 73 (64) IR (KBr) cm-1: 1733, 1643, 1600 1H-NMR (CDCl3) delta: 0.32 (18H, s), 2.64 (2H, t, J=8 Hz), 2.95 (2H, t, J=8 Hz), 3.68 (3H, s), 7.22 (2H, A2B2, J=8.5 Hz), 7.58 (2H, A2B2, J=8.5 Hz), 7.72 (1H, br s, NH), 7.82 (1H, dd, J=1, 1 Hz), 7.93 (2H, d, J=1 Hz) The above methyl ester (556 mg, 1.30 mmol) was dissolved in methanol-DME-water (3:2:1, 9 ml), the solution was added with lithium hydroxide monohydrate (LiOH H2O, 82 mg, 1.95 mmol), and the mixture was refluxed by heating for 2 hours. The reaction mixture was cooled on ice, and then added with aqueous hydrochloric acid (1 N, 2.00 ml, 2.00 mmol), and the mixture was extracted with ethyl acetate. The organic layer was washed with water, and dried over anhydrous sodium sulfate, then the solvent was evaporated, and the residue was recrystallized to obtain the title compound (522 mg, 97%) as colorless prisms. Mp: 151-152C (dichloromethane-hexane) MS (m/z): 413 (M+, 22), 398 (3), 249 (100), 221 (9), 133 (7), 83 (9), 73 (71) IR (KBr) cm-1: 1706, 1639 1H-NMR (CDCl3) delta: 0.31 (18H, s), 2.69 (2H, t, J=7.5 Hz), 2.97 (2H, t, J=7.5 Hz), 7.23 (2H, A2B2, J=8.5 Hz), 7.59 (2H, A2B2, J=8.5 Hz), 7.78 (1H, br s, NH), 7.81 (1H, dd, J=1, 1 Hz), 7.93 (2H, d, J=1 Hz)
88% Example 22; 4-(3,5-Bistrimethylsilanylbenzolyamino)phenylpropionic acid; A solution of 3,5-bis(trimethylsilyl)benzoic acid (120 mg, 0.451 mmol) and cyanuric chloride (125 mg, 0.678 mmol) in acetone (4 ml) was cooled on ice, and added with triethylamine (251 mul, 1.80 mmol), and the mixture was stirred for 5 minutes. The mixture was further stirred at room temperature for 3.5 hours, and then added with <strong>[35418-07-6]methyl 3-(4-aminophenyl)propionate</strong> (121 mg, 0.676 mmol), and the mixture was further stirred for 16 hours. The reaction mixture was added with saturated aqueous sodium hydrogencarbonate, the mixture was extracted with ethyl acetate, the organic layer was treated in a conventional manner, and then the residue was separated by silica gel chromatography [eluted with benzene-ethyl acetate (14:1)], and recrystallized to obtain methyl 4-(3,5-bistrimethylsilanylbenzolyamino)phenylpropionate (169 mg, 88%) as colorless scales.Mp: 119-120.5 C. and 136-137 C. (dichloromethane-hexane)MS (m/z): 427 (M+, 25), 249 (100), 221 (9), 73 (64)IR (KBr) cm-1: 1733, 1643, 16001H-NMR (CDCl3) delta: 0.32 (18H, s), 2.64 (2H, t, J=8 Hz), 2.95 (2H, t, J=8 Hz), 3.68 (3H, s), 7.22 (2H, A2B2, J=8.5 Hz), 7.58 (2H, A2B2, J=8.5 Hz), 7.72 (1H, br s, NH), 7.82 (1H, dd, J=1, 1 Hz), 7.93 (2H, d, J=1 Hz)
 

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