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Details

Stereochemistry ACHIRAL
Molecular Formula C9H10O4
Molecular Weight 182.1733
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of SYRINGALDEHYDE

SMILES

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

InChI

InChIKey=KCDXJAYRVLXPFO-UHFFFAOYSA-N
InChI=1S/C9H10O4/c1-12-7-3-6(5-10)4-8(13-2)9(7)11/h3-5,11H,1-2H3

HIDE SMILES / InChI

Molecular Formula C9H10O4
Molecular Weight 182.1733
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Polyacetylenes and anti-hepatitis B virus active constituents from Artemisia capillaris.
2014-06
1-[3-Meth-oxy-4-(prop-2-yn-1-yl-oxy)phen-yl]ethanone.
2010-12-18
(3E,5E)-3,5-Bis(4-hy-droxy-3,5-di-methoxy-benzyl-idene)oxan-4-one monohydrate.
2010-11-27
Maple syrup phytochemicals include lignans, coumarins, a stilbene, and other previously unreported antioxidant phenolic compounds.
2010-11-24
Enzymatic grafting of simple phenols on flax and sisal pulp fibres using laccases.
2010-11
2-(4-Formyl-2,6-dimeth-oxy-phenoxy)-acetic acid.
2010-10-31
The Ve-mediated resistance response of the tomato to Verticillium dahliae involves H2O2, peroxidase and lignins and drives PAL gene expression.
2010-10-26
Characteristics of lignin from flax shives as affected by extraction conditions.
2010-10-20
2-Amino-4-(4-hy-droxy-3,5-dimeth-oxy-phen-yl)-6-phenyl-nicotinonitrile.
2010-10-09
Bis[4-hy-droxy-3,5-dimeth-oxy-benzalde-hyde (2,4-dinitro-phen-yl)hydrazone] N,N-dimethyl-formamide disolvate monohydrate.
2010-09-30
Biobleaching of eucalypt kraft pulp with a two laccase-mediator stages sequence.
2010-09
Molecular characteristics of Kraft-AQ pulping lignin fractionated by sequential organic solvent extraction.
2010-08-16
Radiosensitization and growth inhibition of cancer cells mediated by an scFv antibody gene against DNA-PKcs in vitro and in vivo.
2010-08-12
Degradation of triclosan by an integrated nano-bio redox process.
2010-08
Miscanthus x giganteus bark organosolv fractionation: fate of lipophilic components and formation of valuable phenolic byproducts.
2010-07-28
[Phenol constituents of Pachysandra terminalis and their antioxidant activity].
2010-07
Synthesis and antioxidant activity evaluation of a syringic hydrazones family.
2010-07
Volatiles from a rare Acer spp. honey sample from Croatia.
2010-06-24
Inhibitory effects of whisky congeners on IgE-mediated degranulation in rat basophilic leukemia RBL-2H3 cells and passive cutaneous anaphylaxis reaction in mice.
2010-06-23
Oxidative depolymerization of lignin in ionic liquids.
2010-06-21
Rapid linkage of indole carboxylic acid to the plant cell wall identified as a component of basal defence in Arabidopsis against hrp mutant bacteria.
2010-06
A new approach to the biobleaching of flax pulp with laccase using natural mediators.
2010-06
Determination of Eucalyptus spp lignin S/G ratio: a comparison between methods.
2010-06
A functional metagenomic approach for expanding the synthetic biology toolbox for biomass conversion.
2010-04-13
Biodegradability of kraft mill TCF biobleaching effluents: application of enzymatic laccase-mediator system.
2010-04
Individual and interaction effects of vanillin and syringaldehyde on the xylitol formation by Candida guilliermondii.
2010-03
Enhanced transformation of triclosan by laccase in the presence of redox mediators.
2010-01
Biology by design: from top to bottom and back.
2010
Capillary electrophoretic determination of selected phenolic compounds in humic substances of well waters and fertilizers.
2010
Coumarins and phenolic fingerprints of oak and Brazilian woods extracted by sugarcane spirit.
2009-11
Bioactivity-guided isolation of cytotoxic constituents from stem-bark of Premna tomentosa.
2009-10-01
Halogenated pesticide transformation by a laccase-mediator system.
2009-10
Effects of biomass hydrolysis by-products on oleaginous yeast Rhodosporidium toruloides.
2009-10
Influence of very low doses of mediators on fungal laccase activity - nonlinearity beyond imagination.
2009-09-04
Effect of metal ions on reactive dye decolorization by laccase from Ganoderma lucidum.
2009-08-30
Characterization of a rare triterpenoid and minor phenolic compounds in the root bark of Anisophyllea dichostyla R. Br.
2009-08
Detoxification of model phenolic compounds in lignocellulosic hydrolysates with peroxidase for butanol production from Clostridium beijerinckii.
2009-07
Fate of grape flavor precursors during storage on yeast lees.
2009-06-24
[Study on chemical constituents from roots of Saussurea lappa].
2009-05
Liquid-liquid extraction of fermentation inhibiting compounds in lignocellulose hydrolysate.
2009-04-01
Cyclooxygenase-2 inhibitory and antioxidant compounds from the truffle Elaphomyces granulatus.
2009-04
Enhanced transformation of malachite green by laccase of Ganoderma lucidum in the presence of natural phenolic compounds.
2009-02
Phenolic constituents from the stem bark of Magnolia officinalis.
2009-01
Phytophenols in whisky lower blood acetaldehyde level by depressing alcohol metabolism through inhibition of alcohol dehydrogenase 1 (class I) in mice.
2008-12
Soluble and insoluble solids contributions to high-solids enzymatic hydrolysis of lignocellulose.
2008-12
Engineering and Applications of fungal laccases for organic synthesis.
2008-11-20
Comparative study of the efficiency of synthetic and natural mediators in laccase-assisted bleaching of eucalyptus kraft pulp.
2008-11
Optimised recovery of lignin-derived phenols in a Scottish fjord by the CuO oxidation method.
2008-10
Homologous cloning, expression, and characterisation of a laccase from Streptomyces coelicolor and enzymatic decolourisation of an indigo dye.
2008-06
Effect of furfural, vanillin and syringaldehyde on Candida guilliermondii growth and xylitol biosynthesis.
2008-03
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:58:22 GMT 2025
Edited
by admin
on Mon Mar 31 19:58:22 GMT 2025
Record UNII
2ZR01KTT21
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
SYRINGALDEHYDE
MI  
Systematic Name English
4-HYDROXY-3,5-DIMETHOXYBENZALDEHYDE
FHFI  
Preferred Name English
NSC-41153
Code English
CEDAR ALDEHYDE
Common Name English
GALLALDEHYDE 3,5-DIMETHYL ETHER
Common Name English
BENZALDEHYDE, 4-HYDROXY-3,5-DIMETHOXY-
Systematic Name English
3,5-DIMETHOXY-4-HYDROXYBENZALDEHYDE
Systematic Name English
SYRINGALDEHYDE [MI]
Common Name English
4-FORMYL-2,6-DIMETHOXYPHENOL
Systematic Name English
2,6-DIMETHOXY-4-FORMYLPHENOL
Systematic Name English
4-HYDROXY-3,5-DIMETHOXYBENZALDEHYDE [FHFI]
Common Name English
FEMA NO. 4049
Code English
Code System Code Type Description
FDA UNII
2ZR01KTT21
Created by admin on Mon Mar 31 19:58:22 GMT 2025 , Edited by admin on Mon Mar 31 19:58:22 GMT 2025
PRIMARY
PUBCHEM
8655
Created by admin on Mon Mar 31 19:58:22 GMT 2025 , Edited by admin on Mon Mar 31 19:58:22 GMT 2025
PRIMARY
CAS
134-96-3
Created by admin on Mon Mar 31 19:58:22 GMT 2025 , Edited by admin on Mon Mar 31 19:58:22 GMT 2025
PRIMARY
CHEBI
67380
Created by admin on Mon Mar 31 19:58:22 GMT 2025 , Edited by admin on Mon Mar 31 19:58:22 GMT 2025
PRIMARY
EPA CompTox
DTXSID2059643
Created by admin on Mon Mar 31 19:58:22 GMT 2025 , Edited by admin on Mon Mar 31 19:58:22 GMT 2025
PRIMARY
MERCK INDEX
m10415
Created by admin on Mon Mar 31 19:58:22 GMT 2025 , Edited by admin on Mon Mar 31 19:58:22 GMT 2025
PRIMARY Merck Index
ECHA (EC/EINECS)
205-167-5
Created by admin on Mon Mar 31 19:58:22 GMT 2025 , Edited by admin on Mon Mar 31 19:58:22 GMT 2025
PRIMARY
WIKIPEDIA
SYRINGALDEHYDE
Created by admin on Mon Mar 31 19:58:22 GMT 2025 , Edited by admin on Mon Mar 31 19:58:22 GMT 2025
PRIMARY
NSC
41153
Created by admin on Mon Mar 31 19:58:22 GMT 2025 , Edited by admin on Mon Mar 31 19:58:22 GMT 2025
PRIMARY
JECFA MONOGRAPH
1856
Created by admin on Mon Mar 31 19:58:22 GMT 2025 , Edited by admin on Mon Mar 31 19:58:22 GMT 2025
PRIMARY