U.S. Department of Health & Human Services Divider Arrow National Institutes of Health Divider Arrow NCATS

Details

Stereochemistry ACHIRAL
Molecular Formula C9H10O3
Molecular Weight 166.1739
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of VERATRALDEHYDE

SMILES

COC1=C(OC)C=C(C=O)C=C1

InChI

InChIKey=WJUFSDZVCOTFON-UHFFFAOYSA-N
InChI=1S/C9H10O3/c1-11-8-4-3-7(6-10)5-9(8)12-2/h3-6H,1-2H3

HIDE SMILES / InChI

Molecular Formula C9H10O3
Molecular Weight 166.1739
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Ligninolysis by a purified lignin peroxidase.
1993 Jun 15
Characterization of aryl alcohol oxidase produced by dye-decolorizing fungus, Geotrichum candidum Decl.
2001
A new cyclobutane lignan from Cinnamomum balansae.
2001
Reactions with pyrrolidine-2,4-diones, Part 4: Synthesis of some 3-substituted 1,5-diphenylpyrrolidine-2,4-diones as potential antimicrobial, anti-HIV-1 and antineoplastic agents.
2001 Dec
Antioxidant properties of 8.0.4'-neolignans.
2001 Nov
Influence of aromatic compounds on biodegradation of [14C]-labeled xylan and mannan by the white-rot fungus Phlebia radiata.
2002 Mar
[Dependence of activities of polysaccharide hydrolases and oxidases from Cerrena unicolor on the source of carbon and aromatic acids in culture media].
2002 May-Jun
Isolation and characterization of aromatics-degrading microorganisms from the gut of the lower termite Coptotermes formosanus.
2003 Apr
Enzyme production by Mycena galopus mycelium in artificial media and in Picea sitchensis F1 horizon needle litter.
2003 Aug
Properties and functional significance of Saccharomyces cerevisiae ADHVI.
2003 Feb 1
Electroenzymatic oxidation of veratryl alcohol by lignin peroxidase.
2003 May 8
Lignin peroxidase-catalyzed oxidation of nonphenolic trimeric lignin model compounds: fragmentation reactions in the intermediate radical cations.
2003 Nov 14
Mechanistic features of lignin peroxidase-catalyzed oxidation of substituted phenols and 1,2-dimethoxyarenes.
2003 Oct 10
Identification of phenolics for control of Aspergillus flavus using Saccharomyces cerevisiae in a model target-gene bioassay.
2004 Dec 29
First synthesis of a polysaccharide-supported lignin model compound and study of its oxidation promoted by lignin peroxidase.
2004 Jan 2
Methyl jasmonate modulated biotransformation of phenylpropanoids to vanillin related metabolites using Capsicum frutescens root cultures.
2005 Feb
Involvement of lipid peroxidation in the degradation of a non-phenolic lignin model compound by manganese peroxidase of the litter-decomposing fungus Stropharia coronilla.
2005 May 6
Asymmetric synthesis of tetrahydropalmatine via tandem 1,2-addition/cyclization.
2005 Nov 11
Tetramethylammonium hydroxide (TMAH) thermochemolysis of lignin: behavior of 4-O-etherified cinnamyl alcohols and aldehydes.
2005 Nov 16
Alpha-monodeuterated benzyl alcohols and phosphobetaines from reactions of aromatic aldehydes with a water/D2O-soluble phosphine.
2006 Dec 11
Targeting antioxidative signal transduction and stress response system: control of pathogenic Aspergillus with phenolics that inhibit mitochondrial function.
2006 Jul
Enhanced activity of strobilurin and fludioxonil by using berberine and phenolic compounds to target fungal antioxidative stress response.
2007 Aug
Combinatorial synthesis and characterization of new asymmetric porphyrins as potential photosensitizers in photodynamic therapy.
2007 Jul
A reliable quantitative method for the analysis of phenolic compounds in Brazilian propolis by reverse phase high performance liquid chromatography.
2007 Nov
Determination of some aldehydes by using solid-phase microextraction and high-performance liquid chromatography with UV detection.
2007 Nov-Dec
A convenient allylsilane-N-acyliminium route toward indolizidine and quinolizidine alkaloids.
2007 Oct 2
Synthesis, structure, electrochemistry, and spectral characterization of bis-isatin thiocarbohydrazone metal complexes and their antitumor activity against ehrlich ascites carcinoma in swiss albino mice.
2008
(E)-3-(3,4-Dimethoxy-phen-yl)-1-(2-thien-yl)prop-2-en-1-one.
2008 Jul 9
The total synthesis of fukiic acid, an HIV-1 integrase inhibitor.
2008 Oct
3-(3,4-Dimethoxy-phenyl)-1-(3-pyridyl)prop-2-en-1-one monohydrate.
2009 Apr 18
Tumor-specific cytotoxic activity of 1,2,3,4-tetrahydroisoquinoline derivatives against human oral squamous cell carcinoma cell lines.
2009 Aug
A validated reverse-phase HPLC analytical method for the quantification of phenolic compounds in Baccharis dracunculifolia.
2009 Jan-Feb
N,N'-Bis(3,4-dimethoxy-benzyl-idene)butane-1,4-diamine.
2009 Jul 4
Diisopropyl 3-[(E)-2-(3,4-dimethoxy-phen-yl)ethen-yl]-5-oxocyclo-hex-3-ene-1,1-dicarboxyl-ate.
2009 May 7
Oxidative cleavage of diverse ethers by an extracellular fungal peroxygenase.
2009 Oct 23
Methyl 5,6-dimeth-oxy-1H-indole-2-carboxyl-ate.
2009 Sep 5
(E)-N'-(3,4-Dimethoxy-benzyl-idene)-2,4-dihydroxy-benzohydrazide methanol solvate.
2009 Sep 9
Inhibition of Escherichia coli glycosyltransferase MurG and Mycobacterium tuberculosis Gal transferase by uridine-linked transition state mimics.
2010 Apr 1
4-Chloro-N-[(E)-(3,4-dimeth-oxy-phen-yl)methyl-idene]aniline.
2010 Aug 18
N'-(3,4-Dimeth-oxy-benzyl-idene)benzo-hydrazide.
2010 Dec 18
Photoenhanced degradation of veratraldehyde upon the heterogeneous ozone reactions.
2010 Jul 21
(2E)-3-(3,4-Dimeth-oxy-phen-yl)-1-(2,5-dimethyl-thio-phen-3-yl)prop-2-en-1-one.
2010 Jul 31
2',3,4,4'-Tetra-meth-oxy-chalcone.
2010 Jun 26
Dimethyl 4-(3,4-dimethoxy-phen-yl)-2,6-dimethyl-1,4-dihydro-pyridine-3,5-dicarboxyl-ate.
2010 May 15
Racemization-free synthesis of (S)-(+)-tylophorine from L-proline by radical cyclization.
2010 May 7
(E)-3,5-Dimeth-oxy-benzaldehyde oxime.
2010 Oct 2
(E)-2-(3,4-Dimeth-oxy-benzyl-idene)-5,6-dimeth-oxy-2,3-dihydro-1H-inden-1-one.
2010 Oct 20
Parameters of Reserpine Analogs That Induce MSH2/MSH6-Dependent Cytotoxic Response.
2010 Sep 13
(E)-1-(2,5-Dichloro-3-thien-yl)-3-(3,4-dimeth-oxy-phen-yl)prop-2-en-1-one.
2010 Sep 4
Enhanced activity of antifungal drugs using natural phenolics against yeast strains of Candida and Cryptococcus.
2011 May
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 16:57:17 GMT 2023
Edited
by admin
on Fri Dec 15 16:57:17 GMT 2023
Record UNII
UI88P68JZD
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
VERATRALDEHYDE
FCC   FHFI   MI  
Systematic Name English
VERATRIC ALDEHYDE
Common Name English
BENZALDEHYDE, 3,4-DIMETHOXY-
Systematic Name English
VERATRALDEHYDE [FCC]
Common Name English
VANILLIN METHYL ETHER
Systematic Name English
NSC-24521
Code English
3,4-DIMETHOXYBENZALDEHYDE
Systematic Name English
VERAPAMIL HYDROCHLORIDE IMPURITY G [EP IMPURITY]
Common Name English
VERAPAMIL RELATED COMPOUND E [USP-RS]
Common Name English
VERATRALDEHYDE [MI]
Common Name English
VERATRALDEHYDE [FHFI]
Common Name English
NSC-8500
Code English
PROTOCATECHUIC ALDEHYDE DIMETHYL ETHER
Common Name English
PROTOCATECHUALDEHYDE DIMETHYL ETHER
Systematic Name English
FEMA NO. 3109
Code English
VERAPAMIL RELATED COMPOUND E
USP-RS  
Common Name English
3,4-DIMETHOXYBENZENECARBONAL
Common Name English
VERAPAMIL RELATED COMPOUND E [USP IMPURITY]
Common Name English
Classification Tree Code System Code
JECFA EVALUATION VERATRALDEHYDE
Created by admin on Fri Dec 15 16:57:17 GMT 2023 , Edited by admin on Fri Dec 15 16:57:17 GMT 2023
CFR 21 CFR 172.515
Created by admin on Fri Dec 15 16:57:17 GMT 2023 , Edited by admin on Fri Dec 15 16:57:17 GMT 2023
Code System Code Type Description
JECFA MONOGRAPH
821
Created by admin on Fri Dec 15 16:57:17 GMT 2023 , Edited by admin on Fri Dec 15 16:57:17 GMT 2023
PRIMARY
RS_ITEM_NUM
1711439
Created by admin on Fri Dec 15 16:57:17 GMT 2023 , Edited by admin on Fri Dec 15 16:57:17 GMT 2023
PRIMARY
CHEBI
17098
Created by admin on Fri Dec 15 16:57:17 GMT 2023 , Edited by admin on Fri Dec 15 16:57:17 GMT 2023
PRIMARY
MERCK INDEX
m11415
Created by admin on Fri Dec 15 16:57:17 GMT 2023 , Edited by admin on Fri Dec 15 16:57:17 GMT 2023
PRIMARY Merck Index
FDA UNII
UI88P68JZD
Created by admin on Fri Dec 15 16:57:17 GMT 2023 , Edited by admin on Fri Dec 15 16:57:17 GMT 2023
PRIMARY
PUBCHEM
8419
Created by admin on Fri Dec 15 16:57:17 GMT 2023 , Edited by admin on Fri Dec 15 16:57:17 GMT 2023
PRIMARY
ECHA (EC/EINECS)
204-373-2
Created by admin on Fri Dec 15 16:57:17 GMT 2023 , Edited by admin on Fri Dec 15 16:57:17 GMT 2023
PRIMARY
SMS_ID
300000032738
Created by admin on Fri Dec 15 16:57:17 GMT 2023 , Edited by admin on Fri Dec 15 16:57:17 GMT 2023
PRIMARY
CAS
120-14-9
Created by admin on Fri Dec 15 16:57:17 GMT 2023 , Edited by admin on Fri Dec 15 16:57:17 GMT 2023
PRIMARY
NSC
8500
Created by admin on Fri Dec 15 16:57:17 GMT 2023 , Edited by admin on Fri Dec 15 16:57:17 GMT 2023
PRIMARY
NSC
24521
Created by admin on Fri Dec 15 16:57:17 GMT 2023 , Edited by admin on Fri Dec 15 16:57:17 GMT 2023
PRIMARY
WIKIPEDIA
VERATRALDEHYDE
Created by admin on Fri Dec 15 16:57:17 GMT 2023 , Edited by admin on Fri Dec 15 16:57:17 GMT 2023
PRIMARY
EPA CompTox
DTXSID7026285
Created by admin on Fri Dec 15 16:57:17 GMT 2023 , Edited by admin on Fri Dec 15 16:57:17 GMT 2023
PRIMARY
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP