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Chemical Structure| 22532-62-3 Chemical Structure| 22532-62-3
Chemical Structure| 22532-62-3

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Product Details of 4-Bromo-2-hydroxybenzaldehyde

CAS No. :22532-62-3
Formula : C7H5BrO2
M.W : 201.02
SMILES Code : O=CC1=CC=C(Br)C=C1O
MDL No. :MFCD06252606
InChI Key :HXTWKHXDFATMSP-UHFFFAOYSA-N
Pubchem ID :4066019

Safety of 4-Bromo-2-hydroxybenzaldehyde

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

Application In Synthesis of 4-Bromo-2-hydroxybenzaldehyde

* 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 [ 22532-62-3 ]

[ 22532-62-3 ] Synthesis Path-Downstream   1~7

  • 1
  • [ 67-66-3 ]
  • [ 591-20-8 ]
  • [ 22532-62-3 ]
  • [ 22532-60-1 ]
  • 2
  • [ 75-25-2 ]
  • [ 591-20-8 ]
  • [ 22532-62-3 ]
  • [ 22532-60-1 ]
  • 3
  • [ 67-66-3 ]
  • [ 591-20-8 ]
  • [ 22532-62-3 ]
  • [ 22532-61-2 ]
  • [ 22532-60-1 ]
  • 4
  • [ 22532-62-3 ]
  • [ 1099-45-2 ]
  • [ 19063-56-0 ]
  • 5
  • [ 22532-62-3 ]
  • [ 96-34-4 ]
  • [ 19063-56-0 ]
  • 7
  • [ 22532-62-3 ]
  • [ 280752-78-5 ]
 

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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 • General Reactivity • Grignard Reaction • Halogenation of Phenols • Hantzsch Dihydropyridine Synthesis • Henry Nitroaldol Reaction • Hiyama Cross-Coupling Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Hydrogenolysis of Benzyl Ether • Julia-Kocienski Olefination • Kinetics of Alkyl Halides • Knoevenagel Condensation • Kumada Cross-Coupling Reaction • 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 Alkyl Halides with Reducing Metals • Reactions of Amines • Reactions of Benzene and Substituted Benzenes • Reactions of Dihalides • Reformatsky Reaction • Reimer-Tiemann Reaction • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Stetter Reaction • Stille Coupling • Stobbe Condensation • Substitution and Elimination Reactions of Alkyl Halides • Suzuki Coupling • Tebbe Olefination • Ugi Reaction • Vilsmeier-Haack Reaction • Wittig Reaction • Wolff-Kishner Reduction

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