Biosynthese und Synthese von Sekundärmetaboliten aus den

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From Wikipedia, the free encyclopedia Cinnamyl alcohol or styron is an organic compound that is found in esterified form in storax, Balsam of Peru, and cinnamon leaves. It forms a white crystalline solid when pure, or a yellow oil when even slightly impure. It can be produced by the hydrolysis of storax. IR Spectrum Table by Frequency Range. 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.

Cinnamyl alcohol ir spectrum

In this lab we will reduce cinnamaldehyde to cinnamyl alcohol using sodium borohydride. The cinnamyl alcohol should smell a little like a hyacinth. Be sure to Please interpret the NMR spectrum shown below. 1. Draw the 8.

104-65-4. Cinnamyl alcohol, formate. Cinnamyl methanoate.

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CAS Registry Number: 103-54-8. Chemical structure: Se hela listan på webbook.nist.gov cinnamic alcohol gamma-phenylallyl alcohol 3-phenyl-2-propen-1-ol: Molecular Formula: C 9 H 10 O: Molecular Weight: 134.2: InChI: InChI=1S/C9H10O/c10-8-4-7-9-5-2-1-3-6-9/h1-7,10H,8H2/b7-4+ InChIKey: OOCCDEMITAIZTP-QPJJXVBHSA-N: RN: 104-54-1: Related pages: Mass MS-NW-1701 13 C NMR NMR-CDS-03-607 1 H NMR NMR-HSP-03-043 IR : liquid film IR-NIDA-04735 IR : CCl 4 solution IR-NIDA-08248 GC-MS Spectrum 1671 - Coniferyl alcohol (HMDB0012915) GC-MS Spectrum 30501 - Coniferyl alcohol (HMDB0012915) GC-MS Spectrum 31567 - Coniferyl alcohol (HMDB0012915) GC-MS Spectrum 32118 - Coniferyl alcohol (HMDB0012915) Cinnamyl formate.

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InChI. InChI=1S/C8H8O/c9-7-6-8-4-2-1-3-5-8/h1-7,9H/b7-6+. InChIKey.

It forms a white crystalline solid when pure, or a yellow oil when even slightly impure. It can be produced by the hydrolysis of storax. Cinnamyl alcohol causes Friedel Crafts alkylation of bulky aromatic compound 2,4-di-tert-butylphenol using mesoporous aluminosilicate as catalyst. Cinnamyl alcohol undergoes partial oxidation in air to form cinnamaldehyde over a series of Bi-Pt/alumina catalysts. Cinnamyl alcohol is used in perfumery and in deodorant compositions. The bark oil consists of cinnamaldehyde (80–90 %), eugenol, eugenol acetate, cinnamyl acetate, cinnamyl alcohol, methyl eugenol, benzaldehyde, cinnamaldehyde, benzyl benzoate, linalool, monoterpene, hydrocarbon, caryophyllene, safrole and others such as pinene, phyllandrene, cymene and cineol.
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Compare the IR spectra of cinnamyl alcohol and cinnamaldehyde.

IR spectrum of cinnamyl alcohol: Type: data: Subject: Spectral data: Spectral Code: If more spectra are required for some specific purpose or commercial use, you Cinnamyl alcohol is a primary alcohol comprising an allyl core with a hydroxy substituent at the 1-position and a phenyl substituent at the 3-position (geometry of the C=C bond unspecified). It has a role as a plant metabolite. Compound Cinnamyl alcoholwith free spectra: 2 FTIR, and 1 Raman. cinnamyl alcohol cinnamic alcohol IR : liquid film IR-NIDA-04735 However we request visitors to our database not to download more than 50 spectra and/or The bark oil consists of cinnamaldehyde (80–90 %), eugenol, eugenol acetate, cinnamyl acetate, cinnamyl alcohol, methyl eugenol, benzaldehyde, cinnamaldehyde, benzyl benzoate, linalool, monoterpene, hydrocarbon, caryophyllene, safrole and others such as pinene, phyllandrene, cymene and cineol.
Branschindex scb

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Biosynthese und Synthese von Sekundärmetaboliten aus den

Linear Formula CH 3 OC 6 H 4 CH 2 OH . Molecular Weight 138.16 . Beilstein/REAXYS Number 636654 . EC Number 203-273-6. MDL number MFCD00004653. PubChem Substance ID 24848301.

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Due to the low levels found in cinnamon, cinnamyl alcohol is usually supplied as [DB14184] within commercial products. Cinnamyl alcohol has been shown to be a skin sensitizer, with a NOEL (No Effect Level) of ~4%. ChemicalBook ProvideCinnamyl alcohol(104-54-1) 1H NMR,IR2,MS,IR3,IR1,1H NMR,Raman,ESR,13C NMR,Spectrum Cinnamyl alcohol causes Friedel Crafts alkylation of bulky aromatic compound 2,4-di-tert-butylphenol using mesoporous aluminosilicate as catalyst. Cinnamyl alcohol undergoes partial oxidation in air to form cinnamaldehyde over a series of Bi-Pt/alumina catalysts. Cinnamyl alcohol is used in perfumery and in deodorant compositions. 2021-03-01 · The signal of pure liquid cinnamyl aldehyde was recorded in the Bruker Vertex 70V spectrometer using the attenuated total reflection infrared (ATR-IR). The spectroscopy was equipped with a DLaTGS detector.

characterization in a mutant pine deficient in cinnamyl alcohol In addition, the terpenes showing this trend, except α-thujene, were oxygenated compounds (alcohols or ketones), and therefore might be produced as the result av M Lang · 2002 · Citerat av 1 — lengruppe bei δ 39-40; die korrespondierenden Signale im Spektrum einer Verbindung mit IR. (KBr): ν~ = 3326 cm-1 (s, br.), 2966 (s), 2920 (ss), 2855 (s), 1668 (w), 1446.