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trans-Cinnamic Acid
SpectraBase Compound ID 3qQUCKKT1iQ
InChI InChI=1S/C9H8O2/c10-9(11)7-6-8-4-2-1-3-5-8/h1-7H,(H,10,11)/b7-6+
InChIKey WBYWAXJHAXSJNI-VOTSOKGWSA-N
Mol Weight 148.16 g/mol
Molecular Formula C9H8O2
Exact Mass 148.052429 g/mol
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Technique FILM (CAST FROM ACETONE)
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Catalog Number C0353
Technique KBr1
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Technique KBr-Pellet
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Technique KBr-Pellet
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Technique KBr-Pellet
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Source of Sample Fluka
Technique KBr pellet
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Source of Sample MCB MANUFACTURING CHEMISTS, NORWOOD, OHIO
Technique KBr WAFER
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Catalog Number W228818
Technique Mull
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Catalog Number W228818
Technique Between salts
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Catalog Number W228818
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Source of Spectrum Sigma-Aldrich Co. LLC.
Catalog Number W228826
Technique Mull
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Source of Sample TCI Chemicals India Pvt. Ltd.
Source of Spectrum Bio-Rad Laboratories, Inc.
Catalog Number C0353
Copyright Copyright © 1980, 1981-2024 John Wiley & Sons, Inc. All Rights Reserved.
Source of Sample Polysciences, Inc., Warrington, Pennsylvania
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Source of Sample TCI Chemicals India Pvt. Ltd.
Source of Spectrum Bio-Rad Laboratories, Inc.
Catalog Number C0353
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Source of Sample Aldrich
Catalog Number 133760
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Source of Sample Aldrich
Catalog Number C80857
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Source of Sample Aldrich
Catalog Number W228818
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Source of Sample Tokyo Kasei Kogyo Company, Ltd., Tokyo, Japan
Solvent CDCl3; Reference=TMS; Temperature 297K
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Solvent CDCl3
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Solvent CDCl3
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Catalog Number C80857
Solvent CDCl3
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Source of Sample Aldrich
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Catalog Number C80857
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Source of Spectrum Sigma-Aldrich Co. LLC.
Catalog Number C80857
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Source of Sample MCB Manufacturing Chemists, Norwood, Ohio
Solvent Polysol; Reference=TMS Spectrometer= Varian CFT-20
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Source of Sample Tokyo Kasei Kogyo Company, Ltd., Tokyo, Japan
Solvent Chloroform-d; Reference=TMS Spectrometer= Bruker AC-300
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Solvent CDCl3 chloroform-d
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Solvent CDCl3
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Solvent CDCl3
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Solvent CDCl3
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Solvent CD3OD
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Solvent CDCl3/DMSO-D6
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Solvent CDCl3
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Solvent CDCl3
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Solvent CDCl3
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Solvent CD3OD
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Solvent CDCl3/DMSO-D6
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Solvent CDCl3
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Solvent CDCl3
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Solvent CDCl3
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Solvent CD3OD
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Solvent CDCl3/DMSO-D6
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Solvent CDCl3
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Solvent CDCl3
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Solvent CDCl3
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Solvent CD3OD
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Solvent CDCl3/DMSO-D6
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Solvent CDCl3
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Solvent CDCl3
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Solvent CDCl3
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Solvent CD3OD
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Solvent CDCl3/DMSO-D6
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Solvent H2O
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Solvent CF3COOH
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Solvent CDCl3
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Solvent ACETANHYDRIDE
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Solvent CDCl3
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Solvent DMSO-D6
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Solvent CDCl3
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Solvent CDCl3
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent CDCl3
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Solvent CD3OD
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Solvent D2O
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Source of Sample Sigma-Aldrich Co. LLC.
Source of Spectrum Sigma-Aldrich Co. LLC.
Catalog Number C80857
Solvent CDCl3
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Source of Spectrum Chemical Concepts, A Wiley Division, Weinheim, Germany
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Source of Spectrum Chemical Concepts, A Wiley Division, Weinheim, Germany
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Source of Spectrum DigiLab GmbH (C) 2024
Technique GC/MS
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Source of Spectrum DigiLab GmbH (C) 2024
Technique GC/MS
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Source of Spectrum DigiLab GmbH (C) 2024
Technique GC/MS
Copyright Database Compilation Copyright © 2023-2024 John Wiley and Sons, Inc. Copyright © 2023-2024 John Wiley and Sons, Inc., Portions Copyright Wiley-VCH GmbH, Adams Library under license from Diablo Analytical. All Rights Reserved.
Source of Spectrum Adams' Essential Oil Components (GC-MS), Version 4
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Source of Spectrum Prof. L. Mondello (Chromaleont s.r.l./Univ. Messina, Italy)
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Source of Spectrum Adams' Essential Oil Components (GC-MS), Version 4
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Source of Spectrum AA-0-851-1
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Source of Spectrum AD-0-2532-0
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Source of Spectrum SWG-33-4822-0
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Source of Spectrum QA-46-611-16
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Source of Spectrum QA-46-611-16
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Source of Spectrum G4-74-627-627-1
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Source of Spectrum U2-2021-SM9-Figure S12
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Source of Spectrum G4-76-69-Cinnamic acid
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Source of Spectrum AD-0-5030-0
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Source of Spectrum EP-8894-0-0
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Source of Spectrum AA-0-852-2
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Source of Spectrum UT-1990-1688-0
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Source of Spectrum WS-1986-92-0
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Source of Spectrum O-2-3263-0
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Source of Spectrum O-15-173-1
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Source of Spectrum J-58-6370-1
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Source of Spectrum SK-32-1612-3
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Source of Spectrum H-87-762-0
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Source of Spectrum G4-70-1033-C
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Source of Spectrum G4-71-2002-D
Copyright Copyright © 2016-2024 W. Robien, Inst. of Org. Chem., Univ. of Vienna. All Rights Reserved.
Solvent ACETONE
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Solvent Acetone
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Solvent Methanol
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Solvent Methanol
  • trans-3-Phenylacrylic acid
  • TRANS-ZIMTSAEURE
  • E-Cinnamic acid
  • ZIMTSAEURE
  • WBYWAXJHAXSJNI-VOTSOKGWSA-N
  • CINNAMIC-ACID;MAJOR-COMPONENT
  • CINNAMOIC-ACID
  • E-3-PHENYL-2-PROPENOIC-ACID
  • Cinnamic acid
  • CINNAMIC ACID, trans-,
  • trans-3-PHENYL-2-PROPENOIC ACID
  • 2-Propenoic acid,3-phenyl
  • Cinnamic acid<E->
  • 2-Propenoic acid, 3-phenyl-, (E)-
  • (e)-3-phenylacrylic acid
  • 3-Phenyl-2-propenoic acid
  • 3-phenylprop-2-enoic acid
Title Journal or Book Year
Bioassay-Guided Fractionation of Melastoma malabathricum Linn. Leaf Solid Phase Extraction Fraction and Its Anticoagulant Activity Molecules 2015
Chemical Constituents of Caesalpinia decapetala (Roth) Alston Molecules 2013
Electronic effects on13C NMR chemical shifts of substituted 1,3,4-thiadiazolium salts Magnetic Resonance in Chemistry 2001
Effect of Substituteents on the 1H and 13C NMR Chemical Shift of trans-Pyridineacrylic and Substituted trans-Cinnamic Acids HETEROCYCLES 1994
Photochromic systems. Part 1. Structural and spectroscopic study of photochromically active products of Stobbe condensation. 2,3-Dibenzylidenesuccinic acid and its anhydride Canadian Journal of Chemistry 1990
17O NMR spectroscopy: Effect of substituents on chemical shifts forp-substituted benzoic acids, methyl benzoates, cinnamic acids and methyl cinnamates Organic Magnetic Resonance 1984
13C substituent effects in monosubstituted benzenes Organic Magnetic Resonance 1979
Nuclear magnetic resonance and structure of hygromycin (homomycin). Agricultural and Biological Chemistry 1978
10.1002/(sici)1097-458x(199703)35:3<159::aid-omr51>3.3.co;2-g "" ""

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