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Chemical Structure| 394-50-3 Chemical Structure| 394-50-3
Chemical Structure| 394-50-3

*Storage: Inert atmosphere,Room Temperature.

3-Fluorosalicylaldehyde

CAS No.: 394-50-3

4.5 *For Research Use Only !

Cat. No.: A689864 Purity: 97%

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Product Details of [ 394-50-3 ]

CAS No. :394-50-3
Formula : C7H5FO2
M.W : 140.11
SMILES Code : O=CC1=CC=CC(F)=C1O
MDL No. :MFCD00003319
InChI Key :NWDHTEIVMDYWQJ-UHFFFAOYSA-N
Pubchem ID :587788

Safety of [ 394-50-3 ]

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

Application In Synthesis [ 394-50-3 ]

* 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 [ 394-50-3 ]

[ 394-50-3 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 394-50-3 ]
  • [ 363-52-0 ]
  • 3
  • [ 1006-67-3 ]
  • [ 394-50-3 ]
  • (Z)-3-fluoro-2-hydroxy-N-(3-oxo-3-phenylprop-1-en-1-yl)benzamide [ No CAS ]
 

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Technical Information

• Acidity of Phenols • Alkyl Halide Occurrence • Barbier Coupling Reaction • Baylis-Hillman Reaction • Benzylic Oxidation • Birch Reduction • Blanc Chloromethylation • Bucherer-Bergs Reaction • Chan-Lam Coupling Reaction • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Chaykovsky Reaction • Corey-Fuchs 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 • Hantzsch Dihydropyridine Synthesis • Henry Nitroaldol Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Hydrogenolysis of Benzyl Ether • Julia-Kocienski Olefination • Knoevenagel Condensation • Leuckart-Wallach Reaction • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Mukaiyama Aldol Reaction • Nozaki-Hiyama-Kishi Reaction • Oxidation of Phenols • Passerini Reaction • Paternò-Büchi Reaction • Pechmann Coumarin Synthesis • Petasis Reaction • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Aldehydes and Ketones • Preparation of Alkylbenzene • Preparation of Amines • Prins Reaction • Reactions of Aldehydes and Ketones • Reactions of Amines • Reactions of Benzene and Substituted Benzenes • Reformatsky Reaction • Reimer-Tiemann Reaction • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Stetter Reaction • Stobbe Condensation • Tebbe Olefination • Ugi Reaction • Vilsmeier-Haack Reaction • Wittig Reaction • Wolff-Kishner Reduction

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