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It has a role as a plant metabolite. Cinnamyl alcohol is a naturally occurring compound that is found within cinnamon. CINNAMYL ALCOHOL, BENZOATE: Source of Sample: R. Kirrstetter, University of Kiel, Kiel, Germany: Copyright: Copyright © 1980, 1981-2020 John Wiley & Sons, Inc. All Rights Reserved. Formula: C16H14O2: InChI: InChI=1S/C16H14O2/c17-16(15-11-5-2-6-12-15)18-13-7-10-14-8-3-1-4-9-14/h1-12H,13H2: InChIKey: UARVBDPGNUHYQT-UHFFFAOYSA-N: Melting Point: 42C: Molecular Weight: 238.29 258 °C Food and Agriculture Organization of the United Nations Cinnamyl alcohol: 250 °C OU Chemical Safety Data (No longer updated) More details: 257-258 °C Alfa Aesar A13025: 250 °C Oakwood: 250 °C … Cinnamyl alcohol 98% Synonym: 3-Phenyl-2-propen-1-ol CAS Number 104-54-1. Linear Formula C 6 H 5 CH=CHCH 2 OH . Molecular Weight 134.18 . Beilstein/REAXYS Number 1903999 .

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Cinnamyl alcohol (2b): Colorless liquid, 1H NMR (CDCl 3 , 400 MHz) δ: 7.40-7.42 (d, J = 8 Hz, 2H), 7.32-7.36 (m, 2H), 7.23-7.29 (m, 1H), 6.62-6.66 (d, J = 16 Hz, 1H), 6.36-6.42 (m, Cinnamyl Alcohol Odor Description: Warm-balsamic, floral-hyacinth and rose, sweet, mild almonds Arctander says this: “Widely used in perfume compositions, including many low-cost floral fragrances, soap perfumes, etc. Blends excellently with Amylsalicylate, Phenylethylalcohol, aromatic … Yield: 37%; 1H NMR (300 MHz, DMSO-d 6) δ: 8.4-8.18 (m, 2H), 8.09-7.9 (m, 2H), 7.68 (d, J = 15.9 Hz, 1H), 6.73 (d, J = 16.2 Hz, 1H) ppm; 13C NMR (75 MHz, DMSO-d 6) δ: 167.03, 147.96, 141.34, 140.75, 129.29, 123.93, 123.61 ppm. Electronic Supplementary Material (ESI) for Green Chemistry This journal is © The Royal Society of Chemistry 2012 Cinnamyl Alcohol. Cinnamyl Alcohol bmse010256 - Data.

Close. 4- acetylpyridene · Adamantane · 2-aminoacetophenone · m-anisaldehyde · benzaldehyde  Biochemistry. NMR characterization of altered lignins extracted from tobacco plants down-regulated for lignification enzymes cinnamyl- alcohol dehydrogenase  C10 H12 O2. NMR Predictor: Predict (works with chrome or firefox) Recommendation for 4-methoxycinnamyl alcohol usage levels up to: not for fragrance  A small extent of lignin condensation (35%) was explained by the high content of cinnamyl alcohol structures, evidenced by 13CNMR-DEPT.

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Cinnamyl Alcohol (C9 H10 O) Cinnamyl Alcohol bmse010256 - Data. bmse010256 Data. Entry STAR file: bmse010256.str. NMR-STAR interactive viewer.

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Using a 3-dimensional similarity model of this enzyme, a series of novel phosphonates (1-5) was designed as potential inhibitors. Phosphonates 1-5 were synthesized in good yield by reacti … 1995-08-01 Cinnamyl alcohol oxidizes rapidly upon air exposure.[Pubmed:23421457] Contact Dermatitis. 2013 Mar;68(3):129-38. BACKGROUND: Cinnamyl alcohol and cinnamal are frequent fragrance contact allergens.

Identify their structures from the 1H NMR and IR spectra given. a) IHD = 5 b) The mass spectrum shows large M+ and (M-CH3) peaks.
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Assign All Signals On The 1H NMR Spectrum Below (letters A-G) To Specific Hydrogen Environments In The Provided Structure. (Ignore The CDCl3 Solvent Peak)  cinnamyl alcohol. CAS No. : 104-54-1 Formula : C9H10O Molecular Weight. : 134.175 Check Encyclopedia. Provied information about Cinnamyl alcohol(Molecular Formula: C9H10O, CAS Registry Number:104-54-1 ) ,Boiling Point,Melting Point,Flash Point,Density,  Apr 8, 2010 FooDB Name, trans-Cinnamyl alcohol This could make trans-cinnamyl alcohol a potential biomarker for the NMR, Not Available.

The scent  mixed with cinnamyl alcohol in the presence or absence of morpholine, shifts in the 1H NMR spectrum indicate coordination of the alcohol with the Lewis acid. The biotransformation of cinnamyl alcohol is investigated using the plant NMR (Nuclear Magnetic Resonance) spectra were measured on a Bruker AMX 300  Cinnamyl alcohol contains total 20 atom(s); 10 Hydrogen atom(s), 9 Carbon atom (s) and 1 Oxygen atom(s). Learn more about cinnamyl alcohol molecular weight at Mol-Instincts. IR spectra · NMR spectra · VCD spectra  av N Selander · 2010 — monitored the borylation of cinnamyl alcohol (41a) and cinnamyl acetate.
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The products were characterised by GC-MS and 1 H NMR. The isolation and characterisation of products obtained from cinnamyl alcohol, 1, using [P 8881 Molbase Encyclopedia provides cinnamyl alcohol (104-54-1) basic information, physical and chemical properties, safety information, toxicity, customs data, synthetic routes, maps, MSDS, generation methods and uses, and its upstream and downstream products, find cinnamyl alcohol … The 1 H spectrum of cinnamyl alcohol (measured on a 500 MHz NMR) is below.. a. Assign all signals on the 1 H NMR spectrum below (letters A-G) to specific hydrogen environments in the provided structure.

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1999-01-01 NMR Characterization of Altered Lignins Extracted from Tobacco Plants Down-Regulated for Lignification Enzymes Cinnamyl-Alcohol Dehydrogenase and Cinnamoyl-CoA Reductase November 1998 • Cinnamic alcohol • Cinnamic alcohol (natural) • Cinnamyl alcohol • EINECS 203-212-3 • FEMA No. 2294 • HSDB 5011 • NSC 8775 • Phenyl-2-propen-1-ol • Propenoic acid, 3-phenyl-, (trans)-• Styrone • Styryl alcohol • Styryl carbinol • Zimtalcohol • gamma-Phenylallyl alcohol .

1 H NMR 2. 13 C NMR 1. Transmission IR 3. Vapor Phase IR 1. Technique. 1H NMR 13C NMR Transmission IR Vapor Phase IR. previous. next.