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[ CAS No. 103986-07-8 ] {[proInfo.proName]}

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Chemical Structure| 103986-07-8
Chemical Structure| 103986-07-8
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Product Details of [ 103986-07-8 ]

CAS No. :103986-07-8 MDL No. :MFCD00090259
Formula : C11H11NO2 Boiling Point : -
Linear Structure Formula :- InChI Key :ITMIUTVFOTYMOJ-UHFFFAOYSA-N
M.W : 189.21 Pubchem ID :3702610
Synonyms :

Safety of [ 103986-07-8 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P312-P321-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 103986-07-8 ]

* 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 [ 103986-07-8 ]

[ 103986-07-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 33906-30-8 ]
  • [ 78-93-3 ]
  • [ 103986-07-8 ]
YieldReaction ConditionsOperation in experiment
39% In acetic acid; for 3.5h;Heating / reflux; <strong>[33906-30-8]2-hydrazinobenzoic acid hydrochloride</strong> (5.00 g, 26.51 mmol) and 2-butanone (10 ml, 110 mmol) in ACOH (50 ml) was refluxed for 3.5 h. Most of solvent evaporated and crude compound dissolved in water/EtOAc. Organic layer evaporated and crude material recryst. in ETOH. Yield 1.96 g (39%). Mp. 216 C. IH NMR (400 MHz, DMSO-d6) 8 2.16 (s, 3 H), 2.36 (s, 3 H), 7.02 (t, J=8 Hz, 1 H), 7.62 (m, 2 H), 10.50 (s, 1 H). 13C NMR (100 MHz, DMSO-d6) 8 8.14, 11.12, 105.53, 112.33, 117. 52, 122.52, 122.60, 130.42, 133.18, 134.27, 168.10. CAS: [103986-07-8]
To a suspension of <strong>[33906-30-8]2-hydrazinobenzoic acid hydrochloride</strong> (2.0 g) in acetic acid (8 ml) was added dropwise a solution of 2-butanone (0.9 ml) in acetic acid (2 ml), and the resultant mixture was heated at 80 C. for one hour.. After 6N-hydrochloric acid (8 ml) was added to the reaction mixture, the mixture was heated at 100 C. for 5 hours.. The mixture was diluted with water (18 ml), and allowed to cool to 40 C. The resultant precipitate was collected by filtration, washed with a small amount of diisopropyl ether and dried in vacuo to give 2,3-dimethyl-1H-indole-7-carboxylic acid (0.78 g). APCI-mass m/z: 190 (M+1) NMR (DMSO-d6, delta); 2.17(3H, s), 2.36 (3H, s), 7.02 (1H, t, d=7.6 Hz), 7.63 (2H, d, d=7.6 Hz), 10.55 (1H, brs), 12.82 (1H, brs).
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