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Chemical Structure| 116096-90-3 Chemical Structure| 116096-90-3

Structure of 116096-90-3

Chemical Structure| 116096-90-3

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Product Details of [ 116096-90-3 ]

CAS No. :116096-90-3
Formula : C7H5BrO3
M.W : 217.02
SMILES Code : O=CC1=CC(Br)=C(O)C=C1O
MDL No. :MFCD20133738
InChI Key :YIIXIVBXVLTMHQ-UHFFFAOYSA-N
Pubchem ID :13950956

Safety of [ 116096-90-3 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 116096-90-3 ]

* 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 [ 116096-90-3 ]

[ 116096-90-3 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 116096-90-3 ]
  • [ 77-78-1 ]
  • [ 57543-36-9 ]
  • 2
  • [ 116096-90-3 ]
  • [ 76350-90-8 ]
  • 5-((4-bromo-2-formyl-5-((2-methylbiphenyl-3-yl)methoxy)phenoxy)methyl)nicotinonitrile [ No CAS ]
  • 3
  • [ 116096-90-3 ]
  • [ 76350-90-8 ]
  • 5-bromo-2-hydroxy-4-((2-methylbiphenyl-3-yl)methoxy)benzaldehyde [ No CAS ]
YieldReaction ConditionsOperation in experiment
33.9% With di-isopropyl azodicarboxylate; triphenylphosphine; In tetrahydrofuran; at 0 - 20℃; To a solution of (2-methyl-[1,1?-biphenyl]-3-yl)methanol (100 mg, 0.507 mmol) and 5-bromo-2,4-dihydroxybenzaldehyde (100 mg, 0.461 mmol) in tetrahydrofuran (5 mL), triphenylphosphine (145 mg, 0.553 mmol) was added. The reaction mixture was stirred at 0 C. for 15 minutes. Diisopropylazodicarboxylate (0.108 mL, 0.553 mmol) was added dropwise in tetrahydrofuran (5 mL). The reaction mixture was then warmed to room temperature and stirred overnight. The reaction mixture was concentrated and to the residue was added acetonitrile. A light yellow solid precipitated and was collected as the final product 5-bromo-2-hydroxy-4-((2-methyl-[1,1?-biphenyl]-3-yl)methoxy)benzaldehyde (62 mg, 0.156 mmol, 33.9% yield).
 

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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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