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[ CAS No. 1470-79-7 ] {[proInfo.proName]}

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Chemical Structure| 1470-79-7
Chemical Structure| 1470-79-7
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Product Details of [ 1470-79-7 ]

CAS No. :1470-79-7 MDL No. :MFCD00002356
Formula : C13H10O4 Boiling Point : -
Linear Structure Formula :- InChI Key :OKJFKPFBSPZTAH-UHFFFAOYSA-N
M.W : 230.22 Pubchem ID :73852
Synonyms :

Safety of [ 1470-79-7 ]

Signal Word:Warning Class:
Precautionary Statements:P261-P305+P351+P338 UN#:
Hazard Statements:H315-H319-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 1470-79-7 ]

* 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 [ 1470-79-7 ]

[ 1470-79-7 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 4038-15-7 ]
  • [ 1470-79-7 ]
  • 2
  • [ 1470-79-7 ]
  • [ 77-78-1 ]
  • [ 4038-15-7 ]
YieldReaction ConditionsOperation in experiment
1.43 g With potassium carbonate; In acetone; for 8h;Reflux; Synthesis of2,4-dimethoxy-4’-methoxybenzophenone10054] 2.00 g of 2,4-dihydroxy-4’-hydroxybenzophenone,1.95 g of dimethyl sulfate and 2.14 g of potassium carbonate are dissolved in 16.0 g of acetone. The mixture is stirred at reflux temperature for 8 hours. Since then, the mixture is cooled to 25 degrees Celsius and thrther stirred after addition of 80.0 g of water, then extracted with 20.0 g ethyl acetate and the organic phase is washed with watet Thereafter, ethyl acetate is distilled away, and the resultant is purified by silica gel colunm chromatography (ethyl acetate:hexane=3:97). Thereby, 1.43 g of 2, 4-dimethoxy-4’-methoxybenzophenone is obtained.
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Technical Information

? Acidity of Phenols ? Arndt-Eistert Homologation ? Baeyer-Villiger Oxidation ? Barbier Coupling Reaction ? Baylis-Hillman Reaction ? Benzylic Oxidation ? Birch Reduction ? Blanc Chloromethylation ? Bucherer-Bergs Reaction ? Chan-Lam Coupling Reaction ? Clemmensen Reduction ? Corey-Bakshi-Shibata (CBS) Reduction ? Corey-Chaykovsky Reaction ? Electrophilic Substitution of the Phenol Aromatic Ring ? Etherification Reaction of Phenolic Hydroxyl Group ? Fischer Indole Synthesis ? Friedel-Crafts Reaction ? Grignard Reaction ? Halogenation of Phenols ? Henry Nitroaldol Reaction ? Horner-Wadsworth-Emmons Reaction ? Hunsdiecker-Borodin Reaction ? Hydride Reductions ? Hydrogenolysis of Benzyl Ether ? Lawesson's Reagent ? Leuckart-Wallach Reaction ? McMurry Coupling ? Meerwein-Ponndorf-Verley Reduction ? Oxidation of Phenols ? Passerini Reaction ? Paternò-Büchi Reaction ? Pechmann Coumarin Synthesis ? Petasis Reaction ? Peterson Olefination ? Pictet-Spengler Tetrahydroisoquinoline Synthesis ? Preparation of Aldehydes and Ketones ? Preparation of Alkylbenzene ? Preparation of Amines ? Preparation of Carboxylic Acids ? Prins Reaction ? Reactions of Aldehydes and Ketones ? Reactions of Amines ? Reactions of Benzene and Substituted Benzenes ? Reactions of Carboxylic Acids ? Reformatsky Reaction ? Reimer-Tiemann Reaction ? Robinson Annulation ? Schlosser Modification of the Wittig Reaction ? Schmidt Reaction ? Specialized Acylation Reagents-Ketenes ? Stobbe Condensation ? Tebbe Olefination ? Ugi Reaction ? Vilsmeier-Haack Reaction ? Wittig Reaction ? Wolff-Kishner Reduction
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