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Chemical Structure| 84434-05-9 Chemical Structure| 84434-05-9

Structure of 84434-05-9

Chemical Structure| 84434-05-9

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Product Details of [ 84434-05-9 ]

CAS No. :84434-05-9
Formula : C15H10O4S
M.W : 286.30
SMILES Code : O=C(O)COC1=CC(C2=O)=C(SC3=C2C=CC=C3)C=C1
MDL No. :MFCD27965627
InChI Key :LJUKODJASZSKFL-UHFFFAOYSA-N
Pubchem ID :3019853

Safety of [ 84434-05-9 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 84434-05-9 ]

* 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 [ 84434-05-9 ]

[ 84434-05-9 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 84434-05-9 ]
  • [ 119692-59-0 ]
  • [ 1214748-81-8 ]
YieldReaction ConditionsOperation in experiment
With 2,6-di-tert-butyl-4-methyl-phenol; tetrabutylammomium bromide; In ISOPROPYLAMIDE; acetonitrile; for 16.0h;Reflux; Synthesis of TX-5; [0144] Synthesis of acrylic acid 4-{2-hydroxy-3-[2-(9-oxo-9H-thioxanthen-2-yloxy)- acetoxy]-propoxy}-butyl ester:2-[(9-oxo-9H-thioxanthen-2-yl)oxy]-acetic acid was prepared according to EP 1380580 A (GREAT LAKES) .A reaction mixture containing (9-oxo-9H-thioxanthen-2-yloxy) acetic acid (4.0 g, 14 mmol), acetonitrile (55 ml), dimethylacetamide (10 mL), tetrabutylammonium bromide (0.5 g, 1.4 mmol)and 2,6-di-tert-butyl-4- methylphenol (0.03 g, 0.114 mmol) was heated to reflux. At this temperature 4-hydroxybutylacrylate glycidylether (2.3 g, 11.4 mmol) was added and the mixture was allowed to stir at reflux temperature for 16 hours. The mixture was cooled to room temperature and the solvent was evaporated under reduced pressure to provide 8.0 g of a yellow oil. The product was purified on a Prochrom LC80 Column using dichloromethane / ethyl acetate (60/40) as eluent on Kromasil Si60A 10μm, to afford 1.8 g of a yellow oil.
1.8 g With 2,6-di-tert-butyl-4-methyl-phenol; tetrabutylammomium bromide; In acetonitrile; for 16.0h;Reflux; Synthesis of TX-5 Synthesis of acrylic acid 4-{2-hydroxy-3-[2-(9-oxo-9H-thioxanthen-2-yloxy)-acetoxy]-propoxy}-butyl esterA reaction mixture containing (9-oxo-9H-thioxanthen-2-yloxy)acetic acid (4.0 g, 14 mmol), acetonitrile (55 ml), dimethylacetamide (10 mL), tetrabutylammonium bromide (0.5 g, 1.4 mmol) and 2,6-di-tert-butyl-4-methylphenol (0.03 g, 0.114 mmol) was heated to reflux. At this temperature 4-hydroxybutylacrylate glycidylether (2.3 g, 11.4 mmol) was added and the mixture was allowed to stir at reflux temperature for 16 hours. The mixture was cooled to room temperature and the solvent was evaporated under reduced pressure to provide 8.0 g of a yellow oil. The product was purified on a Prochrom LC80 Column using Kromasil Si 60A 10 μm as silica and dichloromethane/ethyl acetate (60/40) as eluent, to afford 1.8 g of a yellow oil.
  • 2
  • [ 84434-05-9 ]
  • [ 128-37-0 ]
  • [ 119692-59-0 ]
  • [ 1214748-81-8 ]
YieldReaction ConditionsOperation in experiment
With tetrabutylammomium bromide; In ISOPROPYLAMIDE; acetonitrile; A reaction mixture containing (9-oxo-9H-thioxanthen-2-yloxy)acetic acid (4.0 g, 14 mmol), acetonitrile (55 ml), dimethylacetamide (10 mL), tetrabutylammonium bromide (0.5 g, 1.4 mmol) and 2,6-di-tert-butyl-4-methylphenol (0.03 g, 0.114 mmol) was heated to reflux. At this temperature 4-hydroxybutylacrylate glycidylether (2.3 g, 11.4 mmol) was added and the mixture was allowed to stir at reflux temperature for 16 hours. The mixture was cooled to room temperature and the solvent was evaporated under reduced pressure to provide 8.0 g of a yellow oil. The product was purified on a Prochrom LC80 Column using Kromasil Si 60A 10 μm as silica and dichloromethane/ethyl acetate (60/40) as eluent, to afford 1.8 g of a yellow oil.
 

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