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[ CAS No. 22717-56-2 ] {[proInfo.proName]}

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Chemical Structure| 22717-56-2
Chemical Structure| 22717-56-2
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Product Details of [ 22717-56-2 ]

CAS No. :22717-56-2 MDL No. :MFCD07780736
Formula : C8H7BrO3 Boiling Point : No data available
Linear Structure Formula :- InChI Key :JEMVEVUWSJXZMX-UHFFFAOYSA-N
M.W : 231.04 Pubchem ID :13983552
Synonyms :

Safety of [ 22717-56-2 ]

Signal Word:Warning Class:
Precautionary Statements:P280-P305+P351+P338-P310 UN#:
Hazard Statements:H302-H315-H319-H332-H335 Packing Group:
GHS Pictogram:

Application In Synthesis of [ 22717-56-2 ]

* 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 [ 22717-56-2 ]

[ 22717-56-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 79756-81-3 ]
  • [ 22717-56-2 ]
  • [ 1364266-91-0 ]
  • 2
  • [ 22717-56-2 ]
  • [ 126717-59-7 ]
  • 1‐(4‐bromo-2-hydroxyphenyl)‐2‐(3‐bromo-6-methoxypyridine-2‐yl)ethanone [ No CAS ]
YieldReaction ConditionsOperation in experiment
91.2% Add 250g of tetrahydrofuran to a three-necked flask at room temperature, add 85g of <strong>[126717-59-7]3-bromo-6-methoxy-2-methylpyridine</strong>, add 25.2g of sodium hydroxide in batches with stirring, warm to 60 C, stir for 40 minutes, slowly a mixed solution of 97.2 g of methyl 4-bromosalicylate and 97.2 g of tetrahydrofuran was added dropwise, and the temperature was controlled at 60 C, and the reaction was stirred for 6 hours with stirring. The reaction was complete by TLC. The temperature was lowered, and the reaction liquid was poured into 1 L of water, suction filtered, and dried to give 153.6 g. Yield 91.2%, purity: 96.0%.
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Technical Information

? Acidity of Phenols ? Acyl Group Substitution ? Alkyl Halide Occurrence ? Appel Reaction ? Benzylic Oxidation ? Birch Reduction ? Blanc Chloromethylation ? Bouveault-Blanc Reduction ? Buchwald-Hartwig C-N Bond and C-O Bond Formation Reactions ? Catalytic Hydrogenation ? Chan-Lam Coupling Reaction ? Chugaev Reaction ? Complex Metal Hydride Reductions ? Corey-Kim Oxidation ? Dess-Martin Oxidation ? Electrophilic Substitution of the Phenol Aromatic Ring ? Ester Cleavage ? Etherification Reaction of Phenolic Hydroxyl Group ? Friedel-Crafts Reaction ? General Reactivity ? Grignard Reaction ? Halogenation of Phenols ? Hiyama Cross-Coupling Reaction ? Hydride Reductions ? Hydrogenolysis of Benzyl Ether ? Jones Oxidation ? Kinetics of Alkyl Halides ? Kumada Cross-Coupling Reaction ? Martin's Sulfurane Dehydrating Reagent ? Mitsunobu Reaction ? Moffatt Oxidation ? Oxidation of Alcohols by DMSO ? Oxidation of Phenols ? Pechmann Coumarin Synthesis ? Preparation of Alcohols ? Preparation of Aldehydes and Ketones ? Preparation of Alkylbenzene ? Preparation of Amines ? Reactions of Alcohols ? Reactions of Alkyl Halides with Reducing Metals ? Reactions of Amines ? Reactions of Benzene and Substituted Benzenes ? Reactions of Dihalides ? Reactions with Organometallic Reagents ? Reimer-Tiemann Reaction ? Ritter Reaction ? Sharpless Olefin Synthesis ? Specialized Acylation Reagents-Carbodiimides and Related Reagents ? Stille Coupling ? Substitution and Elimination Reactions of Alkyl Halides ? Suzuki Coupling ? Swern Oxidation ? Vilsmeier-Haack Reaction
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