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Chemical Structure| 67159-79-9 Chemical Structure| 67159-79-9

Structure of 67159-79-9

Chemical Structure| 67159-79-9

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Product Details of [ 67159-79-9 ]

CAS No. :67159-79-9
Formula : C11H11NO3
M.W : 205.21
SMILES Code : O=C1CC(C)(C)C2=C1C=C([N+]([O-])=O)C=C2
MDL No. :MFCD14705049

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Application In Synthesis of [ 67159-79-9 ]

* 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 [ 67159-79-9 ]

[ 67159-79-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 67159-79-9 ]
  • [ 33906-30-8 ]
  • 2-[<i>N</i>'-(3,3-dimethyl-6-nitro-indan-1-ylidene)-hydrazino]-benzoic acid [ No CAS ]
  • 2
  • [ 67159-79-9 ]
  • [ 33906-30-8 ]
  • 10,10-Dimethyl-3-nitro-5,10-dihydro-indeno[1,2-b]indole-6-carboxylic acid [ No CAS ]
YieldReaction ConditionsOperation in experiment
0.178 g (19%) In formic acid; EXAMPLE 24 10,10-Dimethyl-3-nitro-5,10-dihydro-indeno[1,2-b]indole-6-carboxylic acid 6-Nitro-3,3-dimethyl-1-indanone (0.612 g, 2.98 mmol) [Smith, J. G. et al. Org. Prep. and Proc. Int. 1978, 10(3), 123-131] and <strong>[33906-30-8]2-hydrazinobenzoic acid hydrochloride</strong> (0.562 g, 2.98 mmol) in formic acid (2 mL, 96%) were irradiated for two minutes in a closed cap Teflon vessel of a microwave oven (700 W). The mixture was vacuum filtered, and the crude product was chromatographed (hexane/ethyl acetate 1:1) and triturated with petroleum ether/diethyl ether. Drying in vacuo afforded 0.178 g (19%) of the title compound as a yellow solid: mp 310 C. (dec); 1H NMR (DMSO-d6): delta 13.43 (s, 1H), 11.85 (s, 1H), 8.95 (s, 1H), 8.12 (d, 1H), 7.98 (d, 1H), 7.81 (m, 2H), 7.19 (t, 1H), 1.59 (s, 6H); IR (KBr): 3460, 1670 cm-1; MS (m/z) 322 (M+). Elemental analysis for C18H14N2O4 Calc'd: C, 67.08; H, 4.38; N, 8.69. Found: C, 66.29; H, 4.45; N, 8.37.
 

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