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Chemical Structure| 1065076-49-4 Chemical Structure| 1065076-49-4

Structure of 1065076-49-4

Chemical Structure| 1065076-49-4

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Product Details of [ 1065076-49-4 ]

CAS No. :1065076-49-4
Formula : C9H9FO3
M.W : 184.16
SMILES Code : COC1=CC(C(C)=O)=C(F)C=C1O
MDL No. :MFCD11101445
InChI Key :JTOSXEWSXIZJGX-UHFFFAOYSA-N
Pubchem ID :45933642

Safety of [ 1065076-49-4 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P305+P351+P338

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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