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[ CAS No. 36886-76-7 ] {[proInfo.proName]}

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Chemical Structure| 36886-76-7
Chemical Structure| 36886-76-7
Structure of 36886-76-7 * Storage: {[proInfo.prStorage]}
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Product Details of [ 36886-76-7 ]

CAS No. :36886-76-7 MDL No. :MFCD08276350
Formula : C22H16O5 Boiling Point : -
Linear Structure Formula :- InChI Key :GRIKUIPJBHJPPN-UHFFFAOYSA-N
M.W : 360.36 Pubchem ID :169832
Synonyms :
Chemical Name :3',6'-Dimethoxy-3H-spiro[isobenzofuran-1,9'-xanthen]-3-one

Safety of [ 36886-76-7 ]

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 [ 36886-76-7 ]

* 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.

  • Downstream synthetic route of [ 36886-76-7 ]

[ 36886-76-7 ] Synthesis Path-Downstream   1~13

  • 1
  • [ 36886-76-7 ]
  • 3',6'-dimethoxy-spiro[phthalan-1,9'-xanthen]-3-one; hydrochloride [ No CAS ]
YieldReaction ConditionsOperation in experiment
With hydrogenchloride
  • 2
  • [ 36886-76-7 ]
  • 3',6'-dimethoxy-spiro[phthalan-1,9'-xanthen]-3-one; sulfate [ No CAS ]
YieldReaction ConditionsOperation in experiment
With diethyl ether; ethanol; sulfuric acid
  • 3
  • [ 7647-01-0 ]
  • [ 67-56-1 ]
  • [ 36886-76-7 ]
  • 3,6-dimethoxy-9-(2-methoxycarbonyl-phenyl)-xanthylium; chloride [ No CAS ]
YieldReaction ConditionsOperation in experiment
o-(2-Hydroxy-4-methoxybenzoyl)benzoesaeure, m-Methoxyphenol;
YieldReaction ConditionsOperation in experiment
With hydrogenchloride beim Erhitzen unter Druck;
YieldReaction ConditionsOperation in experiment
With lead dioxide; acetic acid
YieldReaction ConditionsOperation in experiment
With hydrogenchloride; acetic acid at 150 - 160℃; unter Druck;
  • 9
  • [ 77-78-1 ]
  • [ 36886-76-7 ]
YieldReaction ConditionsOperation in experiment
With nitrobenzene
  • 10
  • [ 36886-76-7 ]
  • [ 94-36-0 ]
  • 3',6'-dimethoxy-3-oxo-3H-spiro[isobenzofuran-1,9'-xanthen]-4'-yl benzoate [ No CAS ]
  • [ 1431371-12-8 ]
YieldReaction ConditionsOperation in experiment
1: 35% 2: 16% With tris(bipyridine)ruthenium(II) dichloride hexahydrate; sodium hydrogencarbonate In acetonitrile at 20℃; for 60h; Inert atmosphere; Irradiation; regioselective reaction;
  • 11
  • [ 2321-07-5 ]
  • [ 74-88-4 ]
  • [ 36886-76-7 ]
YieldReaction ConditionsOperation in experiment
65% Stage #1: fluorescein With potassium carbonate In N,N-dimethyl-formamide at 20℃; for 1h; Inert atmosphere; Schlenk technique; Stage #2: methyl iodide In N,N-dimethyl-formamide at 70℃; for 24h; Inert atmosphere; Schlenk technique;
  • 12
  • [ 85-44-9 ]
  • [ 150-19-6 ]
  • [ 36886-76-7 ]
YieldReaction ConditionsOperation in experiment
89% With niobium pentachloride In methanesulfonic acid at 95 - 100℃; for 1h; Inert atmosphere;
71% With Zn0.95*Ti0.05O In neat (no solvent) at 160℃; for 4h; Green chemistry; 2.3 General experimental procedure for fluorescein synthesis General procedure: In a typical experimental procedure, phthalic anhydride (1 mmol), resorcinol (2 mmol) and Zn0.950Ti0.050O (10 mol%) catalyst were heated with constant stirring for 1.33h at 160°C and the progress of the reaction was monitored by TLC. After the completion of reaction, the reaction mixture was dissolved in 1N NaOH (10 mL) and the catalyst was separated using centrifugation. The filtrate was acidified using 1N HCl until the solution was neutralized. During neutralization, the precipitation of the dye was observed which was further purified by recrystallization with methanol.
  • 13
  • [ 77-78-1 ]
  • [ 2321-07-5 ]
  • [ 36886-76-7 ]
YieldReaction ConditionsOperation in experiment
92% Stage #1: fluorescein With potassium carbonate In acetone for 0.5h; Stage #2: dimethyl sulfate In acetone at 50℃; for 4h;
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