sinapyl, alcohol, organic, compound, structurally, related, cinnamic, acid, biosynthetized, phenylpropanoid, biochemical, pathway, immediate, precursor, being, sinapaldehyde, this, phytochemical, monolignols, which, precursor, lignin, lignans, also, biosynthet. Sinapyl alcohol is an organic compound structurally related to cinnamic acid It is biosynthetized via the phenylpropanoid biochemical pathway its immediate precursor being sinapaldehyde This phytochemical is one of the monolignols which are precursor to lignin or lignans 1 It is also a biosynthetic precursor to various stilbenoids and coumarins Sinapyl alcohol NamesPreferred IUPAC name 4 1E 3 Hydroxyprop 1 en 1 yl 2 6 dimethoxyphenolOther names Sinapoyl alcohol 4 Hydroxy 3 5 dimethoxycinnamyl alcoholIdentifiersCAS Number 537 33 7 Y3D model JSmol Interactive imageChEBI CHEBI 64557 NChemSpider 4444145 NECHA InfoCard 100 190 507KEGG C02325 NPubChem CID 5280507UNII 8O6NO04SMV YCompTox Dashboard EPA DTXSID10895025InChI InChI 1S C11H14O4 c1 14 9 6 8 4 3 5 12 7 10 15 2 11 9 13 h3 4 6 7 12 13H 5H2 1 2H3 b4 3 NKey LZFOPEXOUVTGJS ONEGZZNKSA N NSMILES OC C C c1cc OC c O c OC c1PropertiesChemical formula C11H14O4Molar mass 210 226Appearance Colourless solidMelting point 61 to 65 C 142 to 149 F 334 to 338 K Except where otherwise noted data are given for materials in their standard state at 25 C 77 F 100 kPa N verify what is Y N Infobox referencesSee also editSinapinic acid Syringol Syringaldehyde Syringic acid Acetosyringone Sinapine Canolol Phenolic content in wineReferences edit Boerjan Wout Ralph John Baucher Marie 2003 Lignin Biosynthesis Annu Rev Plant Biol 54 519 46 doi 10 1146 annurev arplant 54 031902 134938 PMID 14503002 Retrieved from https en wikipedia org w index php title Sinapyl alcohol amp oldid 1177958701, wikipedia, wiki, book, books, library,
