Home Cart 0 Sign in  

[ CAS No. 28461-49-6 ] {[proInfo.proName]}

,{[proInfo.pro_purity]}
Cat. No.: {[proInfo.prAm]}
Chemical Structure| 28461-49-6
Chemical Structure| 28461-49-6
Structure of 28461-49-6 * Storage: {[proInfo.prStorage]}
Cart0 Add to My Favorites Add to My Favorites Bulk Inquiry Inquiry Add To Cart

Quality Control of [ 28461-49-6 ]

Related Doc. of [ 28461-49-6 ]

Alternatived Products of [ 28461-49-6 ]

Product Details of [ 28461-49-6 ]

CAS No. :28461-49-6 MDL No. :MFCD00111324
Formula : C8H11N3O Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 165.19 Pubchem ID :-
Synonyms :

Safety of [ 28461-49-6 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312+P330-P302+P352+P312-P304+P340+P312-P305+P351+P338-P332+P313-P337+P313-P362-P363-P403+P233-P405-P501 UN#:
Hazard Statements:H302+H312+H332-H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 28461-49-6 ]

* 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 [ 28461-49-6 ]

[ 28461-49-6 ] Synthesis Path-Downstream   1~4

  • 3
  • [ 40624-07-5 ]
  • [ 28461-49-6 ]
  • 11-methyl-2,3,4,5,6,7-hexahydropyridazino[6,1-b]pyrrolo[1,2-a]quinazolin-9(1H)-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
89% With iodine; sodium hydrogencarbonate; In acetonitrile; for 10h;Reflux; General procedure: 2-Aminobenzohydrazide (1.0 mmol), <strong>[40624-07-5]1,7-dichloroheptan-4-one</strong> (182 mg, 1.0 mmol), I2 (13 mg, 0.05 mmol), NaHCO3 (252 mg, 3.0 mmol), and CH3CN (10.0 mL) was added into a dry 25 mL flask. The reaction mixture was stirred at reflux for 10-16 h. After the completion of the reaction as monitored by TLC, the solvent was removed under reduces pressure, and the resulting residue was purified by column chromatography using ethyl acetate and petroleum ether (1:4) as an eluent to give the product 3.
  • 4
  • [ 943835-77-6 ]
  • [ 28461-49-6 ]
  • 5-benzoyl-2-fluoro-10-methyl-8H-phthalazino[1,2-b]quinazolin-8-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
78% With iodine; oxygen; In dimethyl sulfoxide; at 90℃;Green chemistry; 2-Aminobenzohydrazide (76mg, 0.5mmol), 2-(phenylethynyl)benzaldehyde (103mg, 0.5mmol), I2 (25mg, 0.1mmol) were added to a dry reaction flask with high vacuum valve. After three times in vacuum and replacement of oxygen, DMSO (5.0mL) was injected into the mixture. Before reaching completion, the reaction mixture was stirred and heated at 90C under an O2 balloon. The mixture was poured into 50mL water, and the yellow precipitate was formed and collected by filtration. The crude product was purified by chromatography over silica gel to give 3a using ethyl acetate and petroleum ether (1:5) as an eluent.
Same Skeleton Products
Historical Records