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Chemical Structure| 133473-26-4 Chemical Structure| 133473-26-4

Structure of 133473-26-4

Chemical Structure| 133473-26-4

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Product Details of [ 133473-26-4 ]

CAS No. :133473-26-4
Formula : C9H9NO3
M.W : 179.17
SMILES Code : O=CCCC1=CC=CC=C1[N+]([O-])=O
MDL No. :MFCD09028590

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Application In Synthesis of [ 133473-26-4 ]

* 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 [ 133473-26-4 ]

[ 133473-26-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 15121-84-3 ]
  • [ 133473-26-4 ]
YieldReaction ConditionsOperation in experiment
85% With pyridinium chlorochromate; In dichloromethane; at 25℃; for 6h; Example 8: A general experimental procedure for the oxidation of alcohols (4a-e) To a stirred solution of alcohol 8a-e (5 mmol) in dry CH2CI2 (10 mL), Pyridinium chlorochromate (PCC) (10 mmol) was added slowly at 25 °C. It was then stirred for further 6 h. After completion of the reaction (monitored by TLC), it was passed through a short pad of silica gel (230-400 mesh) using CH2CI2 as eluent. The comDined organic layers were concentrated under reduced pressure to give the aldehyde 4a-e which was pure enough to be used in the next step. Example 9: 3-(2-Nitrophenyl)propanal (4a) Yield: 85percent (761 mg); gum; IR (CHCl3): umax 765, 1 166, 1225, 1235, 1454, 1712, 2989, 3123; NMR (200 MHz, CDCl3): delta 2.89 (t, J = 7.3 Hz, 2H), 3.20 (t, J = 7.3 Hz, 2H), 7.28-7.59 (m, 3H), 7.92 (d, J = 7.9, 1 H), 9.82 (s, 1 H); 13C NMR (50 MHz, CDCl3): 25.6, 44.4, 124.9, 127.5, 132.3, 133.1 , 135.7, 199.9; Anal. Calcd for C9H9NO3 requires: C, 60.33; H, 5.06; N, 7.82; found: C, 60.45; H, 5.13; N, 7.91percent
85% With pyridinium chlorochromate; In dichloromethane; at 25℃; for 6h; General procedure: To a stirred solution of alcohol 8a-e (5 mmol) in dry CH2Cl2 (10 mL), Pyridinium chlorochromate (PCC) (10 mmol) was added slowly at 25° C. It was then stirred for further 6 h. After completion of the reaction (monitored by TLC), it was passed through a short pad of silica gel (230-400 mesh) using CH2Cl2 as eluent. The combined organic layers were concentrated under reduced pressure to give the aldehyde 4a-e which was pure enough to be used in the next step
85% With pyridinium chlorochromate; In dichloromethane; at 25℃; for 6h; To a stirred solution of alcohol 8a (5 g, 27.60 mmol) in dry CH2Cl2 (100 mL), PCC (11.9 g, 55.20 mmol) was added slowly at 25° C. It was then stirred for further 6 h. After completion of the reaction (monitored by TLC), it was passed through a short pad of silica gel (230-400 mesh) using CH2Cl2 as eluent. The combined organic layers were concentrated under reduced pressure to give aldehyde 4a (4.2 g) which was pure enough to be used for the next step. [0085] Yield: 85percent; gum; IR (CHCl3): umax 667, 756, 850, 1155, 1215, 1253, 1278, 1345, 1476, 1712, 2989, 3123 cm?1; 1H NMR (200 MHz, CDCl3): delta 2.89 (t, J=7.3 Hz, 2H), 3.20 (t, J=7.3 Hz, 2H), 7.34-7.58 (m, 3H), 7.92 (d, J=7.9, 2H), 9.82 (s, 1H); 13C NMR (50 MHz, CDCl3): 25.6, 44.4, 124.9, 127.5, 132.3, 133.1, 135.7, 199.9; Anal. Calcd for C9H9NO3 requires: C, 60.33; H, 5.06; N, 7.82. found: C, 60.38; H, 5.11; N, 7.76percent.
 

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