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[ CAS No. 51659-96-2 ] {[proInfo.proName]}

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Chemical Structure| 51659-96-2
Chemical Structure| 51659-96-2
Structure of 51659-96-2 * Storage: {[proInfo.prStorage]}
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Product Details of [ 51659-96-2 ]

CAS No. :51659-96-2 MDL No. :
Formula : C7H8Cl2N2O Boiling Point : -
Linear Structure Formula :- InChI Key :-
M.W : 207.06 Pubchem ID :-
Synonyms :

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Application In Synthesis of [ 51659-96-2 ]

* 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 [ 51659-96-2 ]

[ 51659-96-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 123-91-1 ]
  • [ 104566-41-8 ]
  • [ 51659-96-2 ]
  • [ 104565-45-9 ]
YieldReaction ConditionsOperation in experiment
With potassium carbonate; In water; EXAMPLE 1A 4-Chloro-5-(3-benzyloxybenzylamino)-2-i-propyl-3-(2H)pyridazinone (Compound No. 95) STR61 A mixture comprising 8.24 g of <strong>[104566-41-8]3-benzyloxybenzylamine hydrochloride</strong> prepared in Reference Example 2A, 3.11 g of 2-i-propyl-4,5-dichloro-3(2H)pyridazinone, 7.26 g of potassium carbonate, 30 ml of 1,4-dioxane and 90 ml of water was refluxed under stirring for 4.5 hours. The majority of 1,4-dioxane was distilled off under reduced pressure, and the residue was extracted with ethyl acetate. The extract was washed with diluted hydrochloric acid, and then treated with cerite to remove the precipitate. The organic layer was separated, and washed with water and a saturated sodium chloride aqueous solution, and then dried over sodium sulfate. Then, the solvent was distilled off. The pale yellow oily substance thereby obtained was crystallized from ether-n-hexane to obtain 2.51 g of the above identified compound having a melting point of from 106 to 108 C. as colorless crystals. NMR(CDCl3)6: 7.48 (1H, s), 7.30 (5H, s), 7.3-6.7 (4H, m), 5.02 (2H, s), 4.49, 4.40 (total 2H, each s), 5.2-4.8 (1H, broad s), 1.30 (6H, d). MS (m/e): 383(M+), 348, 91 (100%).
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