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Chemical Structure| 35274-53-4 Chemical Structure| 35274-53-4

Structure of 35274-53-4

Chemical Structure| 35274-53-4

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Product Details of [ 35274-53-4 ]

CAS No. :35274-53-4
Formula : C10H11BrO4
M.W : 275.10
SMILES Code : O=CC1=CC(OC)=C(OC)C(OC)=C1Br
MDL No. :MFCD02104429

Safety of [ 35274-53-4 ]

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

Application In Synthesis of [ 35274-53-4 ]

* 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 [ 35274-53-4 ]

[ 35274-53-4 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 19832-98-5 ]
  • [ 35274-53-4 ]
  • 2-(2-bromo-3,4,5-trimethoxybenzylidene)-4-methyl-1-tetralone [ No CAS ]
YieldReaction ConditionsOperation in experiment
69% With sodium hydroxide; In ethanol; at 5 - 27℃; To a round bottom flask containing 15 mL of ethanol were added 4-methyl-tetralone (10 mmol, 1 eq)And 2-bromo-3,4,5-trimethoxybenzaldehyde (10 mmol, 1 eq),The temperature was maintained at 5 C.Thereafter, a 40% solution of sodium hydroxide in ethanol was added.The mixture was stirred at 27 & lt; 0 & gt; C for 1-24 h.The appearance of the precipitate and the color change indicate the formation of the product.The reaction was monitored by TLC.When the reaction is complete, the acidified ice is added to quench the reaction.Followed by recrystallization or column chromatography to obtain the purified product in a yield of 69%.
  • 2
  • [ 19832-98-5 ]
  • [ 35274-53-4 ]
  • 2-(2-bromo-3,4,5-trimethoxy-benzylidene)-4-methyl-tetraloneoxime [ No CAS ]
 

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Technical Information

• Alkyl Halide Occurrence • Barbier Coupling Reaction • Baylis-Hillman Reaction • Bucherer-Bergs Reaction • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Chaykovsky Reaction • Corey-Fuchs Reaction • Fischer Indole Synthesis • General Reactivity • Grignard Reaction • Hantzsch Dihydropyridine Synthesis • Henry Nitroaldol Reaction • Hiyama Cross-Coupling Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • 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 • Nomenclature of Ethers • Nozaki-Hiyama-Kishi Reaction • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Pictet-Spengler Tetrahydroisoquinoline Synthesis • Preparation of Aldehydes and Ketones • Preparation of Amines • Preparation of Ethers • 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 • Reactions of Ethers • Reformatsky 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 • Wittig Reaction • Wolff-Kishner Reduction

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