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Record Information
Version2.0
Created at2020-11-23 19:41:09 UTC
Updated at2021-08-19 23:59:26 UTC
NP-MRD IDNP0002816
Secondary Accession NumbersNone
Natural Product Identification
Common NameSinapyl alcohol
Provided ByBMRBBMRB logo
DescriptionSinapyl alcohol belongs to the class of organic compounds known as methoxyphenols. Methoxyphenols are compounds containing a methoxy group attached to the benzene ring of a phenol moiety. Sinapyl alcohol is a primary metabolite. Primary metabolites are metabolically or physiologically essential metabolites. They are directly involved in an organism’s growth, development or reproduction. Sinapyl alcohol is found in Aeschynanthus bracteatus , Tabernaemontana divaricata, Fagus grandifolia, Populus tremula, Saccharum officinarum, Streptomyces nigra and Wedelia prostrata. Sinapyl alcohol was first documented in 2002 (PMID: 12659499). Based on a literature review very few articles have been published on Sinapyl alcohol.
Structure
Thumb
Synonyms
ValueSource
(e)-Sinapoyl alcoholChEBI
Sinapoyl alcoholChEBI
(e)-Sinapyl alcoholHMDB
(e)-3-(4-Hydroxy-3,5-dimethoxyphenyl)-2-propen-1-olHMDB
4-(3-Hydroxy-1-propenyl)-2,6-dimethoxy-phenolHMDB
4-(3-Hydroxyprop-1-en-1-yl)-2,6-dimethoxyphenolHMDB
4-Hydroxy-3,5-dimethoxycinnamyl alcoholHMDB
Sinapic alcoholHMDB
Sinapyl alcohol(e)HMDB
Sinapyl-alcoholHMDB
trans-Sinapoyl alcoholHMDB
Sinapyl alcoholMeSH
Chemical FormulaC11H14O4
Average Mass210.2265 Da
Monoisotopic Mass210.08921 Da
IUPAC Name4-[(1E)-3-hydroxyprop-1-en-1-yl]-2,6-dimethoxyphenol
Traditional Namesinapyl alcohol
CAS Registry NumberNot Available
SMILES
COC1=CC(\C=C\CO)=CC(OC)=C1O
InChI Identifier
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+
InChI KeyLZFOPEXOUVTGJS-ONEGZZNKSA-N
Experimental Spectra
Spectrum TypeDescriptionDepositor EmailDepositor OrganizationDepositorDeposition DateView
1D NMR1H NMR Spectrum (1D, 500 MHz, DMSO, simulated)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 500 MHz, DMSO, simulated)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
1D NMR13C NMR Spectrum (1D, 500 MHz, DMSO, experimental)Wishart LabWishart LabDavid Wishart2021-06-20View Spectrum
Predicted Spectra
Not Available
Chemical Shift Submissions
Not Available
Species
Species of Origin
Chemical Taxonomy
Description Belongs to the class of organic compounds known as methoxyphenols. Methoxyphenols are compounds containing a methoxy group attached to the benzene ring of a phenol moiety.
KingdomOrganic compounds
Super ClassBenzenoids
ClassPhenols
Sub ClassMethoxyphenols
Direct ParentMethoxyphenols
Alternative Parents
Substituents
  • Cinnamyl alcohol
  • Methoxyphenol
  • Dimethoxybenzene
  • M-dimethoxybenzene
  • Anisole
  • Phenoxy compound
  • Phenol ether
  • Styrene
  • Methoxybenzene
  • Alkyl aryl ether
  • Monocyclic benzene moiety
  • Ether
  • Organooxygen compound
  • Organic oxygen compound
  • Alcohol
  • Primary alcohol
  • Hydrocarbon derivative
  • Aromatic homomonocyclic compound
Molecular FrameworkAromatic homomonocyclic compounds
External Descriptors
Physical Properties
StateNot Available
Experimental Properties
PropertyValueReference
Melting PointNot AvailableNot Available
Boiling Point384.00 to 385.00 °C. @ 760.00 mm Hg (est)The Good Scents Company Information System
Water Solubility17130 mg/L @ 25 °C (est)The Good Scents Company Information System
LogP1.361 (est)The Good Scents Company Information System
Predicted Properties
PropertyValueSource
logP1.36ALOGPS
logP1.2ChemAxon
logS-2.3ALOGPS
pKa (Strongest Acidic)9.4ChemAxon
pKa (Strongest Basic)-2.5ChemAxon
Physiological Charge0ChemAxon
Hydrogen Acceptor Count4ChemAxon
Hydrogen Donor Count2ChemAxon
Polar Surface Area58.92 ŲChemAxon
Rotatable Bond Count4ChemAxon
Refractivity58.1 m³·mol⁻¹ChemAxon
Polarizability22.26 ųChemAxon
Number of Rings1ChemAxon
BioavailabilityYesChemAxon
Rule of FiveYesChemAxon
Ghose FilterYesChemAxon
Veber's RuleNoChemAxon
MDDR-like RuleNoChemAxon
HMDB IDHMDB0013070
DrugBank IDNot Available
Phenol Explorer Compound IDNot Available
FoodDB IDFDB031178
KNApSAcK IDC00002778
Chemspider ID4444145
KEGG Compound IDC02325
BioCyc IDSINAPYL-ALCOHOL
BiGG IDNot Available
Wikipedia LinkSinapyl alcohol
METLIN IDNot Available
PubChem Compound5280507
PDB ID55B
ChEBI ID64557
Good Scents IDrw1282941
References
General References
  1. Bonini C, D'Auria M, Ferri R: Singlet oxygen mediated degradation of lignin--isolation of oxidation products from steam-exploded lignin from pine. Photochem Photobiol Sci. 2002 Aug;1(8):570-3. doi: 10.1039/b202209e. [PubMed:12659499 ]