SpectraBase Spectrum ID: 7YHaS5OvAJ2: SpectraBase Batch ID: JKiLJgiJ31O: Name: 2-PROPEN-1-OL, 3-PHENYL-, CAS Registry Number: 104-54-1: Copyright: Copyright © 1980, 1981-2020 John Wiley & Sons, Inc. All Rights Reserved. Detector Name: TGS/TRIGLYCINE SULFATE/ Formula: C9H10O: InChI: InChI=1S/C9H10O/c10-8-4-7-9-5-2-1-3-6-9/h1-7,10H,8H2: InChIKey: OOCCDEMITAIZTP-UHFFFAOYSA-N
ChemicalBook ProvideCinnamyl alcohol(104-54-1) IR3,IR2,MS,IR3,IR1,1H NMR, Raman,ESR,13C NMR,Spectrum.
Molecular Weight 138.16 . Beilstein/REAXYS Number 636654 . EC Number 203-273-6. MDL number MFCD00004653.
30 The obtained nanotubes exhibited higher activity and selectivity in the hydrogenation of cinnamaldehyde to cinnamyl alcohol, compared with the conventional nanoparticles. 1993-01-01 · The signal (3,350cm-~) for the O-H bond arising from cinnamyl alcohol was not observed. The IH-NMR spectrum indicated the presence of 2 pro- tons of an aromatic ring adjacent to a carbonyl group (7.96-8.10ppm), 8 protons of an aromatic ring (7.33- 7.60 ppm), 2 protons of an alkene (6.30-6.56 ppm) and 2 protons of an alkane (4.96 ppm) as 4-Methoxybenzyl alcohol 98% Synonym: p-Anisyl alcohol, Anis alcohol, Anise alcohol CAS Number 105-13-5. Linear Formula CH 3 OC 6 H 4 CH 2 OH . Molecular Weight 138.16 . Beilstein/REAXYS Number 636654 .
2021-04-10. Create. 2005-03-26. Cinnamyl acetate is an acetate ester resulting from the formal condensation of cinnamyl alcohol with acetic acid. Found in cinnamon leaf oil. It has a role as a fragrance, a metabolite and an insecticide. It derives from a cinnamyl alcohol.
The reaction parameters were optimized and compared in green (water and heptane), blue (toluene, acetonitrile, and cyclohexane), and red (benzene) solvents and molecular oxygen. Cinnamaldehyde is an organic compound with the formula C6H5CH=CHCHO. Occurring naturally as predominantly the trans isomer, it gives cinnamon its flavor and odor.
Compound Cinnamyl alcoholwith free spectra: 2 FTIR, and 1 Raman.
2. Search results for ir spectra at Sigma-Aldrich. Compare Products: Select up to 4 products. *Please select more than one item to compare An Example IR Spectrum Because each interatomic bond may vibrate in several different motions (stretching or bending), individual bonds may absorb at more than one IR frequency. Stretching absorptions usually produce stronger peaks than bending, however the weaker bending absorptions can be useful in differentiating similar types of bonds (e.g. aromatic substitution).
PubChem Substance ID 24850157. NACRES NA.22
This noticeably broadens IR spectral features in the 3,000 cm-1 region.
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2016-09-01 · The experimental results on detection and identification of intermediate radicals and molecular products from gas-phase pyrolysis of cinnamyl alcohol (CnA), the simplest non-phenolic lignin model compound, over the temperature range of 400–800 °C are reported. Cinnamyl alcohol is an organic compound that is found in esterified form in storax, balsam Peru and cinnamon leaves. It forms a white crystalline solid when pure, or a yellow oil when even slightly impure.
Thus, cinnamyl
A very intense observed band at 963 cm −1 in the infrared spectrum of cinnamyl alcohol was calculated to have 50% C C and 22% C O stretching modes . A very intense doublet of bands was observed at 1057 and 1030 cm −1 in the infrared spectrum of 3-phenyl-1-propanol .
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av M Österberg · 2000 · Citerat av 24 — based on polarised infrared spectroscopy measurements, that the cellulose precursors, coniferyl alcohol, p-hydroxy-cinnamic alcohol and sinapyl alcohol [55].
Use this table when you already know the frequency of your material. Find the frequency range in the first column on the left side of the chart and corresponding values in adjacent columns.
2017-06-05 · The catalytic efficiencies of the prepared catalysts were tested for liquid phase oxidation of cinnamyl alcohol (CnOH) to cinnamaldehyde (CnHO) in a modified batch reactor. The reaction parameters were optimized and compared in green (water and heptane), blue (toluene, acetonitrile, and cyclohexane), and red (benzene) solvents and molecular oxygen.
Figure 2.1 Oxidations of benzoic acid. Introduction: Primary alcohols can be oxidized to Sep 12, 2015 Trans- cinnamaldehyde.13C spectrum, IR , NMR. trans-cinnamaldehyde. This 13 C spectrum exhibits resonances at the following chemical Use: The aroma of Cinnamic Alcohol Natural (Styrax Fractions) is fresh, sweet, powdery, cinnamon toast like with a delicate spice finish.
15. 43 (56ak). 12[c]. TMS. 14. 80 (56al). 13. 15.