Home Cart 0 Sign in  

[ CAS No. 25428-06-2 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 25428-06-2
Chemical Structure| 25428-06-2
Structure of 25428-06-2 * Storage: {[proInfo.prStorage]}
Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Quality Control of [ 25428-06-2 ]

Related Doc. of [ 25428-06-2 ]

Alternatived Products of [ 25428-06-2 ]

Product Details of [ 25428-06-2 ]

CAS No. :25428-06-2 MDL No. :MFCD13193690
Formula : C9H11NO Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 149.19 Pubchem ID :-
Synonyms :

Safety of [ 25428-06-2 ]

Signal Word:Warning Class:N/A
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501 UN#:N/A
Hazard Statements:H302-H312-H315-H319-H332-H335 Packing Group:N/A
GHS Pictogram:

Application In Synthesis of [ 25428-06-2 ]

* 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.

  • Upstream synthesis route of [ 25428-06-2 ]
  • Downstream synthetic route of [ 25428-06-2 ]

[ 25428-06-2 ] Synthesis Path-Upstream   1~2

  • 1
  • [ 25428-06-2 ]
  • [ 109-94-4 ]
  • [ 23432-40-8 ]
YieldReaction ConditionsOperation in experiment
53% With hydrogenchloride In water; toluene Example 4
Process for Producing 6-Methyl-4-Quinolone
Toluene (8 mol) was added to 2-amino-5-methylacetophenone (99 mg, 0.67 mmol) to form a solution.
To this solution was added sodium hydride (60percent in oil; 80 mg, 2 mmol), and the mixture was stirred at room temperature for 30 minutes.
Ethyl formate (0.27 ml, 3.3 mmol) was then added, and the mixture was further stirred overnight at room temperature.
After adding water (3 ml) to the reaction solution, and stirring for 5 minutes, 10percent hydrochloric acid was added to the mixture for neutralization, thereby causing precipitation of crystals.
The crystals were collected by filtration, washed with water (3 ml*2), and dried to give 56 mg of the desired product (yield 53percent).
1H-NMR (DMSO-d6, 400 MHz): δ 2.40 (s, 3H), 5.99 (dd, J=1.2, J=7.3 Hz, 1H), 7.41-7.49 (m, 2H), 7.84 (dd, J=5.9, 7.3 Hz, 1H), 7.87 (s, 1H), 11.7 (brs, 1H).
Mass Spectrometry (FD-MS, m/z): 159 (M+).
Reference: [1] Patent: US6187926, 2001, B1,
  • 2
  • [ 107-31-3 ]
  • [ 25428-06-2 ]
  • [ 23432-40-8 ]
Reference: [1] Chemistry - A European Journal, 2015, vol. 21, # 6, p. 2339 - 2342
Same Skeleton Products
Historical Records