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[ CAS No. 20009-28-3 ] {[proInfo.proName]}

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Cat. No.: {[proInfo.prAm]}
Chemical Structure| 20009-28-3
Chemical Structure| 20009-28-3
Structure of 20009-28-3 * Storage: {[proInfo.prStorage]}
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Product Details of [ 20009-28-3 ]

CAS No. :20009-28-3 MDL No. :MFCD04275627
Formula : C13H10O Boiling Point : -
Linear Structure Formula :- InChI Key :RACCOFGYHHVUQB-UHFFFAOYSA-N
M.W : 182.22 Pubchem ID :15689008
Synonyms :

Safety of [ 20009-28-3 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P264-P271-P280-P302+P352-P304+P340-P305+P351+P338-P312-P362-P403+P233-P501 UN#:
Hazard Statements:H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 20009-28-3 ]

* 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 [ 20009-28-3 ]

[ 20009-28-3 ] Synthesis Path-Downstream   1~8

  • 1
  • [ 6165-75-9 ]
  • [ 135-19-3 ]
  • [ 20009-28-3 ]
  • 2
  • [ 23133-37-1 ]
  • [ 20009-28-3 ]
  • 4-[3-(2-naphthyloxy)prop-1-ynyl]-1-propylpiperidin-4-ol [ No CAS ]
YieldReaction ConditionsOperation in experiment
75% Stage #1: naphth-2-yloxymethylacetylene With potassium hydroxide In diethyl ether at 21℃; for 0.5h; Stage #2: 1-propyl-4-piperidone In diethyl ether at 21℃;
  • 3
  • [ 20009-28-3 ]
  • [ 5326-87-4 ]
  • C21H18N4O2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
With sodium azide; copper(ll) sulfate pentahydrate; sodium L-ascorbate In water; N,N-dimethyl-formamide at 50 - 65℃; regioselective reaction; General procedure for the synthesis of amide-ether-linked 1,4-disubstituted 1,2,3-triazoles7a-e, 10a-e and 13a, b, d and e General procedure: For the synthesis of amide-ether-linked 1,4-disubstituted 1,2,3-triazoles, an aqueoussolution of sodium azide (3.0/5.0 mole ratio) was added to a solution of 1.0/2.0 mole ratio of2-bromo-N-substituted acetamides 6a-e and dimethylformamide under stirring at 50-65 °C.Then, terminal alkynes 3, 9 and 12 (1.0 mmol) were added followed by addition of coppersulfate pentahydrate (1.0/2.0 mole ratio) and sodium ascorbate (1.0/2.0 mole ratio). The reactionmixture was stirred for 6-12 h at the same temperature (Schemes 1-3). After completionof the reaction, cold water was added to the reaction mixture and the precipitated solid was filteredoff and washed with aqueous ammonia solution followed by water. The crude productwas purified by washing with ethyl acetate and dried under vacuum to afford the desired 1,4--disubstituted 1,2,3-triazoles (7a-e, 10a-e and 13a, b, d and e) in good yield.
  • 4
  • [ 1072-21-5 ]
  • [ 20009-28-3 ]
  • 1,12-bis(naphthalen-2-yloxy)dodeca-2,10-diyne-4,9-diol [ No CAS ]
YieldReaction ConditionsOperation in experiment
66% Stage #1: naphth-2-yloxymethylacetylene With n-butyllithium In tetrahydrofuran; hexane at -78℃; for 1h; Inert atmosphere; Stage #2: hexanedial In tetrahydrofuran; hexane at -78 - 20℃; for 2h; Inert atmosphere;
  • 5
  • [ 20009-28-3 ]
  • [ 452-68-6 ]
  • 1-(4-fluoro-3-methylphenyl)naphtho[2,1-b]furan-2-carbaldehyde [ No CAS ]
  • 6
  • [ 20009-28-3 ]
  • [ 452-68-6 ]
  • C20H15FO [ No CAS ]
  • 7
  • [ 20009-28-3 ]
  • [ 83846-48-4 ]
  • 1-(3-chloro-4-methylphenyl)naphtho[2,1-b]furan-2-carbaldehyde [ No CAS ]
  • 8
  • [ 20009-28-3 ]
  • [ 83846-48-4 ]
  • C20H15ClO [ No CAS ]
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