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[ CAS No. 5435-40-5 ]

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Chemical Structure| 5435-40-5
Chemical Structure| 5435-40-5
Structure of 5435-40-5 * Storage: {[proInfo.prStorage]}

Quality Control of [ 5435-40-5 ]

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Alternatived Products of [ 5435-40-5 ]
Alternatived Products of [ 5435-40-5 ]

Product Details of [ 5435-40-5 ]

CAS No. :5435-40-5 MDL No. :MFCD02664400
Formula : C12H13NO2 Boiling Point : 426.3°C at 760 mmHg
Linear Structure Formula :- InChI Key :-
M.W :203.24 g/mol Pubchem ID :-
Synonyms :

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Signal Word: Class:
Precautionary Statements: UN#:
Hazard Statements: Packing Group:

Application In Synthesis of [ 5435-40-5 ]

  • Downstream synthetic route of [ 5435-40-5 ]

[ 5435-40-5 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 1196-79-8 ]
  • [ 50-00-0 ]
  • [ 151-50-8 ]
  • [ 5435-40-5 ]
YieldReaction ConditionsOperation in experiment
With ethanol; water at 150℃; unter Druck;
With ethanol; water at 150℃; unter Druck;
  • 2
  • [ 7515-90-4 ]
  • [ 5435-40-5 ]
YieldReaction ConditionsOperation in experiment
With zinc(II) chloride
YieldReaction ConditionsOperation in experiment
67% R.82 2-(2,5-dimethyl-1H-indol-3-yl)acetic acid Reference Example 82 2-(2,5-dimethyl-1H-indol-3-yl)acetic acid Reaction was conducted in the same manner as Reference Example 81, except that 4-methylphenylhydrazine hydrochloride was used instead of 4-trifluoromethoxyphenylhydrazine hydrochloride, to obtain the title compound (67% yield). The NMR data for the obtained compound were as follows. NMR: (300 MHz, DMSO-d6) δ: 2.29 (3H,s), 2.34 (3H,s), 3.51 (2H,s), 6.80 (1H,dd), 7.0-7.2 (2H,m), 11.66 (1H,s), 11.8-12.1 (1H,m)
2,5-Dimethyl-indol, Glykolsaeure, wss. KOH, (250grad, 17h);
(yield)43percent;
YieldReaction ConditionsOperation in experiment
With potassium hydroxide
With potassium hydroxide
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