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[ CAS No. 75433-99-7 ] {[proInfo.proName]}

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Chemical Structure| 75433-99-7
Chemical Structure| 75433-99-7
Structure of 75433-99-7 * Storage: {[proInfo.prStorage]}
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Product Details of [ 75433-99-7 ]

CAS No. :75433-99-7 MDL No. :MFCD08444483
Formula : C11H9NO3 Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 203.19 Pubchem ID :-
Synonyms :

Safety of [ 75433-99-7 ]

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

Application In Synthesis of [ 75433-99-7 ]

* 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.

  • Upstream synthesis route of [ 75433-99-7 ]
  • Downstream synthetic route of [ 75433-99-7 ]

[ 75433-99-7 ] Synthesis Path-Upstream   1~1

  • 1
  • [ 75433-99-7 ]
  • [ 75434-18-3 ]
YieldReaction ConditionsOperation in experiment
97%
Stage #1: at 0 - 125℃;
Stage #2: With ammonia In water
Stage #3: With hydrogenchloride In water
6-Methoxy-quinoline-2-carboxylic acid (4 g, 0.019 mol) was suspended in hydrobromic acid 48percent in water (80 ml) and the mixture was heated at 125° C. overnight.
After cooling to 0° C. ammonium hydroxide was added until the pH was 6-7 followed by addition of HCl until the pH was 3-4 and the compound precipitated.
The solid was filtrated, washed with water and dried under vacuum to yield 3.5 g (0.0185 mol, 97percent of theory) of the title compound as a yellow solid MS (m/e)=190.1 (M+H)+.
Reference: [1] Patent: US2006/84679, 2006, A1, . Location in patent: Page/Page column 12
[2] Patent: US4461896, 1984, A,
[3] Bioorganic and Medicinal Chemistry Letters, 2009, vol. 19, # 15, p. 4495 - 4500
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