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[ CAS No. 637347-67-2 ] {[proInfo.proName]}

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3d Animation Molecule Structure of 637347-67-2
Chemical Structure| 637347-67-2
Chemical Structure| 637347-67-2
Structure of 637347-67-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 637347-67-2 ]

CAS No. :637347-67-2 MDL No. :MFCD20641588
Formula : C8H8ClNO2 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 185.61 Pubchem ID :-
Synonyms :

Safety of [ 637347-67-2 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H302-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 637347-67-2 ]

* 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 [ 637347-67-2 ]

[ 637347-67-2 ] Synthesis Path-Downstream   1~10

  • 1
  • [ 107583-35-7 ]
  • [ 637347-67-2 ]
  • 2
  • [ 34633-67-5 ]
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  • [ 637347-67-2 ]
  • [ 21460-88-8 ]
  • 4
  • [ 637347-67-2 ]
  • [ 60100-09-6 ]
  • [ 860193-30-2 ]
  • 5
  • [ 5162-82-3 ]
  • [ 637347-67-2 ]
  • 6
  • hydroxyimino-acetic acid-(4-chloro-3-methyl-anilide) [ No CAS ]
  • [ 637347-67-2 ]
  • 7
  • [ 637347-67-2 ]
  • 6-chloro-3-[3-(3-hydroxy-[2]piperidyl)-2-oxo-propyl]-7-methyl-3<i>H</i>-quinazolin-4-one [ No CAS ]
  • 8
  • [ 637347-67-2 ]
  • [ 858416-98-5 ]
  • 9
  • [ 637347-67-2 ]
  • [ 857382-39-9 ]
  • 10
  • [ 107583-35-7 ]
  • [ 637347-66-1 ]
  • [ 63329-55-5 ]
  • [ 637347-67-2 ]
YieldReaction ConditionsOperation in experiment
11%; 14% 30% aqueous hydrogen peroxide solution (3.0 ml) was added dropwise over a 5 minute period to a solution of the mixture of isatin isomers (2.00 g, 10.2 mmol) prepared as described in Example 55 (2) above in 2N aqueous sodium hydroxide solution (15 ML). After stirring at room temperature for 1 hour, the reaction mixture was acidified to pH 5 with 1N hydrochloric acid and then concentrated in vacuo. The residue thus obtained was purified by twice- repeated silica gel column chromatography using a 1: 1 by volume mixture of ethyl acetate and hexane as the eluant to yield 5-chloro-4-methylanthranilic acid (271 mg, yield: 14%) as orange-colored crystals from the less polar fraction and 5-CHLORO-6-METHYLANTHRANILIC acid (208 mg, yield: 11%) from the more polar fraction.
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