show-parent-groups. 203-199-4, 104-40-5 Cinnamyl alcohol. 203-212-3, 104-54- Cinnamyl alcohol. 203-212-3 4-methoxybenzyl alcohol.

2004-09-16. 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. Cinnamyl alcohol is a naturally occurring compound that is found within cinnamon.

11(1), 105-125. Abstract In this study, the entire gene encoding cinnamyl alcohol dehydrogenase in kenaf ( HcCAD2 ) was cloned and characterized. gamma-PHENYLALLYL ALCOHOL, ZIMTALCOHOL: Chemical Names: CINNAMYL ALCOHOL: JECFA number: 647: COE number: 65: FEMA number: 2294: Functional Class: Flavouring Agent. FLAVOURING_AGENT Sinapyl alcohol is a primary alcohol, being cinnamyl alcohol hydroxylated at C-4 and methoxylated at C-3 and -5. It has a role as a plant metabolite. It is a primary alcohol, a member of phenols and a dimethoxybenzene.

636), eight related esters (Nos. 637-644), and the corresponding aldehyde (No. 645) and carboxylic acid (No. 646). Cinnamyl alcohol dehydrogenase (CAD) and caffeic acid O-methyltransferase (COMT) catalyze key steps in the pathway of lignin monomer biosynthesis. Brown midrib mutants in Zea mays and Sorghum bicolor with impaired CAD or COMT activity have attracted considerable agronomic interest for their altered lignin composition and improved digestibility.

by reducing cinnamaldehyde either to cinnamyl alcohol OR dihydrocinnamyl Selective reduction of functional groups can also be achieved by chemical

group are primary alcohols, aldehydes, or carboxylic acids, or their corresponding esters and acetals. The primary oxygenated functional group is located on a three-carbonsaturated or unsaturated (i.e~, at the 2,3 position) chain with a benzene ring at the 3 position (i.e., a 3-phenylpropyl or 3-phenyl-2-propenylgroup).

In IUPAC nomenclature, prefixes, suffixes and infixes are used to describe the type and position of functional groups in the substance. If more than one IUPAC name is available from REACH registered dossiers, all IUPAC names are displayed in ‘Other names’ section of the Brief Profile. trans - p -coumaryl alcohol ( CHEBI:64555 ) has functional parent ( E )-cinnamyl alcohol ( CHEBI:33227) coniferol ( CHEBI:17745 ) has functional parent ( E )-cinnamyl alcohol ( CHEBI:33227) IUPAC Name. (2 E )-3-phenylprop-2-en-1-ol. Synonyms.

646). ChEBI Name cinnamyl alcohol: ChEBI ID CHEBI:17177: Definition 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). Cinnamyl alcohol REACH pre-registration, Other, Cosmetic Products Regulation, Annex III - Restricted Substances, Annex II, Sec III - Allergenic Fragrances Banned/Restricted in Toys gamma-Phenylallyl alcohol Structure, properties, spectra, suppliers and links for: Cinnamyl alcohol, 104-54-1, 4407-36-7. (E)-5-hydroxyconiferyl alcohol (CHEBI:31135) has functional parent (E)-cinnamyl alcohol (CHEBI:33227) (E)-caffeyl alcohol (CHEBI:31334) has functional parent (E)-cinnamyl alcohol (CHEBI:33227) 3,4,5-trimethoxy cinnamyl alcohol (CHEBI:86546) has functional parent (E)-cinnamyl alcohol (CHEBI:33227) 3,4-dimethoxycinnamyl alcohol (CHEBI:86551) has functional parent (E)-cinnamyl alcohol (CHEBI:33227) trans-p-coumaryl alcohol (CHEBI:64555) has functional parent (E)-cinnamyl alcohol (CHEBI:33227 A total of 6 dose groups were selected for the study viz. 0 mg/kg bw/day (control group), 250 mg/kg bw (Low Dose Group), 500 mg/kg bw (Intermediate Dose Group) and 1000 mg/kg bw (High Dose Group). Cinnamyl alcohol and cinnamaldehyde derivatives 165 3.3.2. primary oxygenated functional group is located on a three-carbonsaturated or unsaturated (i.e~, "Functional characterization of cinnamyl alcohol dehydrogenase during developmental stages and under various stress conditions in kenaf (Hibiscus cannabinus L.)," BioRes.
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show-parent-groups.

104-54-1. 203-212-3. Förekomst av ämnet måste anges i den för teckning över bestånds delar som avses i artikel 19.1 g om Jan 22, · Skinner H.A., Sheu W.J. Reliability of alcohol use indices.
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Dec 12, 2017 The solubility of cinnamyl alcohol in 11 pure solvents (methanol, ethanol, 21) including functional groups, viscosity, as well as intermolecular

A phylogenetic analysis showed that TaCAD1 belonged to the bona fide CAD group involved This MassBank Record with Accession GLS00145 contains the MS mass spectrum of 'Cinnamyl alcohol' with the InChIKey 'OOCCDEMITAIZTP-QPJJXVBHSA-N'. Answer to: All of the following compounds are aromatic compounds. Identify the functional group of each of the groups attached to the aromatic cinnamyl-alcohol dehydrogenase activity Source: TAIR Ref.2 "Functional reclassification of the putative cinnamyl alcohol dehydrogenase multigene family in Arabidopsis." Cinnamyl alcohol dehydrogenase (CAD) functions in monolignol biosynthesis and plays a critical role in wood development and defense. In this study, we isolated and cloned nine CAD/CAD-like genes Involved in lignin biosynthesis. May catalyze the final step specific for the production of lignin monomers, like coniferyl alcohol, sinapyl alcohol and 4-coumaryl alcohol.1 Publication. "Brown-midrib maize (bm1) -- a mutation affecting the cinnamyl alcohol dehydrogenase gene." 2010-04-16 Question: halogenating cinnamyl alcohol In halogenating the OH functional group in Cinnamyl Alcohol, will it take preference over the double bond between C1-C2? As I want to reduce OH to CH3 without touching the double bond.