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Chemical Structure| 49678-08-2 Chemical Structure| 49678-08-2

Structure of 4-Nitrocinnamaldehyde
CAS No.: 49678-08-2

Chemical Structure| 49678-08-2

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Product Details of [ 49678-08-2 ]

CAS No. :49678-08-2
Formula : C9H7NO3
M.W : 177.16
SMILES Code : O=C/C=C/C1=CC=C([N+]([O-])=O)C=C1
MDL No. :MFCD00007379
InChI Key :ALGQVMMYDWQDEC-OWOJBTEDSA-N
Pubchem ID :5354135

Safety of [ 49678-08-2 ]

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

Application In Synthesis of [ 49678-08-2 ]

* 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 [ 49678-08-2 ]

[ 49678-08-2 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 49678-08-2 ]
  • [ 71510-95-7 ]
  • [ 1345157-71-2 ]
YieldReaction ConditionsOperation in experiment
With (2S)-2-{diphenyl[(trimethylsilyl)oxy]methyl}pyrrolidine; potassium acetate; In 2,2,2-trifluoroethanol; at 20℃; for 14h; General procedure: In a round bottom flask, unsaturated aldehyde 2 (0.25 mmol, 1 equiv), amidomalonate 1 (0.3 mmol, 1.2 equiv), catalyst (0.05 mmol, 20% mol), and KOAc (0.3 mmol, 1.2 equiv) were added sequentially in 1 mL of 2,2,2-trifluoroethanol. The reaction was stirred at room temperature overnight. Then the crude was purified by column chromatography to furnish piperidine adducts 3.
  • 2
  • [ 49678-08-2 ]
  • [ 570-02-5 ]
  • (Z)-3-(2,4,6-trimethoxyphenyl)-3-(4-nitrophenyl)acrylaldehyde [ No CAS ]
  • (E)-3-(2,4,6-trimethoxyphenyl)-3-(4-nitrophenyl)acrylaldehyde [ No CAS ]
  • 3
  • [ 49678-08-2 ]
  • [ 17413-10-4 ]
  • [ 84-11-7 ]
  • (E)-1-((2,3-dihydrobenzo[b][1,4]dioxin-6-yl)methyl)-2-(4-nitrostyryl)-1H-phenanthro[9,10-d]imidazole [ No CAS ]
 

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Technical Information

• Baeyer-Villiger Oxidation • Barbier Coupling Reaction • Baylis-Hillman Reaction • Benzylic Oxidation • Birch Reduction • Blanc Chloromethylation • Bucherer-Bergs Reaction • Clemmensen Reduction • Complex Metal Hydride Reductions • Corey-Bakshi-Shibata (CBS) Reduction • Corey-Chaykovsky Reaction • Corey-Fuchs Reaction • Fischer Indole Synthesis • Friedel-Crafts Reaction • Grignard Reaction • Hantzsch Dihydropyridine Synthesis • Henry Nitroaldol Reaction • Horner-Wadsworth-Emmons Reaction • Hydride Reductions • Hydrogenolysis of Benzyl Ether • Julia-Kocienski Olefination • Knoevenagel Condensation • Lawesson's Reagent • Leuckart-Wallach Reaction • McMurry Coupling • Meerwein-Ponndorf-Verley Reduction • Mukaiyama Aldol Reaction • Nozaki-Hiyama-Kishi Reaction • Passerini Reaction • Paternò-Büchi Reaction • Petasis Reaction • Peterson Olefination • 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 • Robinson Annulation • Schlosser Modification of the Wittig Reaction • Schmidt Reaction • Specialized Acylation Reagents-Ketenes • Stetter Reaction • Stobbe Condensation • Tebbe Olefination • Ugi Reaction • Vilsmeier-Haack Reaction • Wittig Reaction • Wolff-Kishner Reduction

Categories

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