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Chemical Structure| 1963-36-6 Chemical Structure| 1963-36-6
Chemical Structure| 1963-36-6

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4-Methoxycinnamaldehyde (p-Methoxycinnamaldehyde) is an active component of Agastache rugosa with cellular protective effects against respiratory syncytial virus (RSV) in human laryngeal cancer cell lines, effectively inhibiting RSV cytopathogenicity with an IC50 of approximately 0.055 μg/mL.

Synonyms: p-Methoxycinnamaldehyde

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Product Details of 4-Methoxycinnamaldehyde

CAS No. :1963-36-6
Formula : C10H10O2
M.W : 162.19
SMILES Code : O=C/C=C/C1=CC=C(OC)C=C1
Synonyms :
p-Methoxycinnamaldehyde
MDL No. :MFCD00017343
InChI Key :AXCXHFKZHDEKTP-NSCUHMNNSA-N
Pubchem ID :641294

Safety of 4-Methoxycinnamaldehyde

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H315-H319-H335
Precautionary Statements:P233-P260-P261-P264-P271-P280-P302+P352-P304-P304+P340-P305+P351+P338-P312-P321-P332+P313-P337+P313-P340-P362-P403-P403+P233-P405-P501

Application In Synthesis of 4-Methoxycinnamaldehyde

* 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 [ 1963-36-6 ]

[ 1963-36-6 ] Synthesis Path-Downstream   1~2

  • 2
  • [ 1963-36-6 ]
  • [ 2478-38-8 ]
  • 1-(4-hydroxy-3,5-dimethoxyphenyl)-5-(4-methoxyphenyl)-penta-2,4-dien-1-one [ 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 • Nomenclature of Ethers • 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 • Preparation of Ethers • Prins Reaction • Reactions of Aldehydes and Ketones • Reactions of Amines • Reactions of Benzene and Substituted Benzenes • Reactions of Ethers • 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

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