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[ CAS No. 1065076-49-4 ] {[proInfo.proName]}

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Chemical Structure| 1065076-49-4
Chemical Structure| 1065076-49-4
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Product Details of [ 1065076-49-4 ]

CAS No. :1065076-49-4 MDL No. :MFCD11101445
Formula : C9H9FO3 Boiling Point : -
Linear Structure Formula :- InChI Key :JTOSXEWSXIZJGX-UHFFFAOYSA-N
M.W : 184.16 Pubchem ID :45933642
Synonyms :

Safety of [ 1065076-49-4 ]

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
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Application In Synthesis of [ 1065076-49-4 ]

* 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 [ 1065076-49-4 ]

[ 1065076-49-4 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 72955-97-6 ]
  • [ 75-36-5 ]
  • [ 1065076-49-4 ]
YieldReaction ConditionsOperation in experiment
90% Intermediate 1l-(2-Fluoro-4-h droxy-5-methoxyphenyl)ethanone (Dl)To a suspension of AICI3 (1.17g ; 8.79mmol) in 1,2-dichloroethane (2 ml_) was added acetyl chloride (0.55g ; 7.03 mmol). After 10 min stirring was added dropwise a solution of <strong>[72955-97-6]5-fluoro-2-methoxyphenol</strong> (0.50g; 3.52 mmol) in 1,2-dichloroethane (2 ml_) . The reaction mixture was stirred overnight at 40C. The mixtu re was then pou red on iced water and extracted with diethylether. The organic phases were combined, washed FAB-P978PC - 11 Nov 0914with brine, dried (Na2S04) and concentrated to afford 582 mg (90%) of the title compound as an off-white solid .MS (ES) m/e 185(M + H)+ TLC : eluent cyclohexane/EtOAc 7/3 Rf = 0,23
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Technical Information

? Acidity of Phenols ? Alkyl Halide Occurrence ? 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 ? Hydride Reductions ? Hydrogenolysis of Benzyl Ether ? Lawesson's Reagent ? Leuckart-Wallach Reaction ? McMurry Coupling ? Meerwein-Ponndorf-Verley Reduction ? Nomenclature of Ethers ? 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 Ethers ? Prins Reaction ? Reactions of Aldehydes and Ketones ? Reactions of Amines ? Reactions of Benzene and Substituted Benzenes ? Reactions of Ethers ? 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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