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Details

Stereochemistry ACHIRAL
Molecular Formula C11H14O3
Molecular Weight 194.2271
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 4-ALLYL-2,6-DIMETHOXYPHENOL

SMILES

COC1=CC(CC=C)=CC(OC)=C1O

InChI

InChIKey=FWMPKHMKIJDEMJ-UHFFFAOYSA-N
InChI=1S/C11H14O3/c1-4-5-8-6-9(13-2)11(12)10(7-8)14-3/h4,6-7,12H,1,5H2,2-3H3

HIDE SMILES / InChI
Molecular Formula C11H14O3
Molecular Weight 194.2271
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

2013
596
PubMed

PubMed

TitleDatePubMed
Identifying acetylated lignin units in non-wood fibers using pyrolysis-gas chromatography/mass spectrometry.
2004
Chemical characterization of lignin and lipid fractions in kenaf bast fibers used for manufacturing high-quality papers.
2004 Jul 28
CINNAMYL ALCOHOL DEHYDROGENASE-C and -D are the primary genes involved in lignin biosynthesis in the floral stem of Arabidopsis.
2005 Jul
Identification and characterisation of Arabidopsis glycosyltransferases capable of glucosylating coniferyl aldehyde and sinapyl aldehyde.
2005 May 23
Simplified preparation of coniferyl and sinapyl alcohols.
2005 May 4
Molecular requirements of lignin-carbohydrate complexes for expression of unique biological activities.
2005 Sep
Physicochemical model to interpret the kinetics of aroma extraction during wine aging in wood. Model limitations suggest the necessary existence of biochemical processes.
2006 Apr 19
Evidence for a role of AtCAD 1 in lignification of elongating stems of Arabidopsis thaliana.
2006 Dec
Magic-angle spinning NMR studies of cell wall bound aromatic-aliphatic biopolyesters associated with strengthening of intercellular adhesion in potato (Solanum tuberosum L.) tuber parenchyma.
2006 Mar
GOLD HULL AND INTERNODE2 encodes a primarily multifunctional cinnamyl-alcohol dehydrogenase in rice.
2006 Mar
Effects of coumarate 3-hydroxylase down-regulation on lignin structure.
2006 Mar 31
Monolignol oxidation by xylem peroxidase isoforms of Norway spruce (Picea abies) and silver birch (Betula pendula).
2006 May
[Chemical constituents of Myristica fragrans Houttuyn seed and their physiological activities].
2008 Jan
The presence of sinapyl lignin in Ginkgo biloba cell cultures changes our views of the evolution of lignin biosynthesis.
2009 Feb
Fate of grape flavor precursors during storage on yeast lees.
2009 Jun 24
The cinnamyl alcohol dehydrogenase gene family in Populus: phylogeny, organization, and expression.
2009 Mar 6
Spectroscopic analyses of the biofuels-critical phytochemical coniferyl alcohol and its enzyme-catalyzed oxidation products.
2009 Nov 23
Phenolic compounds in ectomycorrhizal interaction of lignin modified silver birch.
2009 Sep 29
Fungal bioconversion of lignocellulosic residues; opportunities & perspectives.
2009 Sep 4
Mass spectrometry-based sequencing of lignin oligomers.
2010 Aug
Molecular characteristics of Kraft-AQ pulping lignin fractionated by sequential organic solvent extraction.
2010 Aug 16
Fast pyrolysis of palm kernel shells: influence of operation parameters on the bio-oil yield and the yield of phenol and phenolic compounds.
2010 Dec
1-[3-Meth-oxy-4-(prop-2-yn-1-yl-oxy)phen-yl]ethanone.
2010 Dec 18
Down-regulation of four putative arabinoxylan feruloyl transferase genes from family PF02458 reduces ester-linked ferulate content in rice cell walls.
2010 Feb
Stone formation in peach fruit exhibits spatial coordination of the lignin and flavonoid pathways and similarity to Arabidopsis dehiscence.
2010 Feb 9
Functional analysis of a cinnamyl alcohol dehydrogenase involved in lignin biosynthesis in wheat.
2010 Jun
Advances in modifying lignin for enhanced biofuel production.
2010 Jun
Identifying new lignin bioengineering targets: 1. Monolignol-substitute impacts on lignin formation and cell wall fermentability.
2010 Jun 17
Arabidopsis peroxidase-catalyzed copolymerization of coniferyl and sinapyl alcohols: kinetics of an endwise process.
2010 Oct
Distribution of lignin-carbohydrate complex in plant kingdom and its functionality as alternative medicine.
2010 Oct
Characteristics of lignin from flax shives as affected by extraction conditions.
2010 Oct 20
The Ve-mediated resistance response of the tomato to Verticillium dahliae involves H2O2, peroxidase and lignins and drives PAL gene expression.
2010 Oct 26
Subdivision of the MDR superfamily of medium-chain dehydrogenases/reductases through iterative hidden Markov model refinement.
2010 Oct 27
Aporphine alkaloids, clerodane diterpenes, and other constituents from Tinospora cordifolia.
2010 Sep
Insights into lignin primary structure and deconstruction from Arabidopsis thaliana COMT (caffeic acid O-methyl transferase) mutant Atomt1.
2010 Sep 7
Substance Class Chemical
Created
by admin
on Fri Dec 15 18:45:18 GMT 2023
Edited
by admin
on Fri Dec 15 18:45:18 GMT 2023
Record UNII
8VF00YWP89
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
4-ALLYL-2,6-DIMETHOXYPHENOL
FHFI  
Systematic Name English
2,6-DIMETHOXY-4-(2-PROPENYL)PHENOL
Systematic Name English
PHENOL, 2,6-DIMETHOXY-4-(2-PROPEN-1-YL)-
Systematic Name English
4-ALLYLSYRINGOL
Common Name English
2,6-DIMETHOXY-4-ALLYLPHENOL
Systematic Name English
4-ALLYL-2,6-DIMETHOXYPHENOL [FHFI]
Common Name English
2,6-DIMETHOXYCHAVICOL
Common Name English
PHENOL, 2,6-DIMETHOXY-4-(2-PROPENYL)-
Systematic Name English
PHENOL, 4-ALLYL-2,6-DIMETHOXY-
Systematic Name English
FEMA NO. 3655
Code English
4-HYDROXY-3,5-DIMETHOXYALLYLBENZENE
Systematic Name English
METHOXYEUGENOL
Systematic Name English
CHAVICOL, 2,6-DIMETHOXY-
Common Name English
NSC-60246
Code English
4-(2-PROPENYL)SYRINGOL
Common Name English
6-METHOXYEUGENOL
Systematic Name English
NSC-16953
Code English
Classification Tree Code System Code
JECFA EVALUATION 4-ALLYL-2,6-DIMETHOXYPHENOL
Created by admin on Fri Dec 15 18:45:18 GMT 2023 , Edited by admin on Fri Dec 15 18:45:18 GMT 2023
Code System Code Type Description
WIKIPEDIA
Methoxyeugenol
Created by admin on Fri Dec 15 18:45:18 GMT 2023 , Edited by admin on Fri Dec 15 18:45:18 GMT 2023
PRIMARY
FDA UNII
8VF00YWP89
Created by admin on Fri Dec 15 18:45:18 GMT 2023 , Edited by admin on Fri Dec 15 18:45:18 GMT 2023
PRIMARY
DAILYMED
8VF00YWP89
Created by admin on Fri Dec 15 18:45:18 GMT 2023 , Edited by admin on Fri Dec 15 18:45:18 GMT 2023
PRIMARY
ECHA (EC/EINECS)
229-600-2
Created by admin on Fri Dec 15 18:45:18 GMT 2023 , Edited by admin on Fri Dec 15 18:45:18 GMT 2023
PRIMARY
JECFA MONOGRAPH
708
Created by admin on Fri Dec 15 18:45:18 GMT 2023 , Edited by admin on Fri Dec 15 18:45:18 GMT 2023
PRIMARY
EPA CompTox
DTXSID30216470
Created by admin on Fri Dec 15 18:45:18 GMT 2023 , Edited by admin on Fri Dec 15 18:45:18 GMT 2023
PRIMARY
NSC
60246
Created by admin on Fri Dec 15 18:45:18 GMT 2023 , Edited by admin on Fri Dec 15 18:45:18 GMT 2023
PRIMARY
CAS
6627-88-9
Created by admin on Fri Dec 15 18:45:18 GMT 2023 , Edited by admin on Fri Dec 15 18:45:18 GMT 2023
PRIMARY
PUBCHEM
226486
Created by admin on Fri Dec 15 18:45:18 GMT 2023 , Edited by admin on Fri Dec 15 18:45:18 GMT 2023
PRIMARY
RXCUI
1423781
Created by admin on Fri Dec 15 18:45:18 GMT 2023 , Edited by admin on Fri Dec 15 18:45:18 GMT 2023
PRIMARY RxNorm
NSC
16953
Created by admin on Fri Dec 15 18:45:18 GMT 2023 , Edited by admin on Fri Dec 15 18:45:18 GMT 2023
PRIMARY
NIH
NCATS
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