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
Enhanced activity of antifungal drugs using natural phenolics against yeast strains of Candida and Cryptococcus.
2011-05
N'-(3,4-Dimeth-oxy-benzyl-idene)benzo-hydrazide.
2010-12-18
(E)-2-(3,4-Dimeth-oxy-benzyl-idene)-5,6-dimeth-oxy-2,3-dihydro-1H-inden-1-one.
2010-10-20
(E)-3,5-Dimeth-oxy-benzaldehyde oxime.
2010-10-02
Parameters of Reserpine Analogs That Induce MSH2/MSH6-Dependent Cytotoxic Response.
2010-09-13
(E)-1-(2,5-Dichloro-3-thien-yl)-3-(3,4-dimeth-oxy-phen-yl)prop-2-en-1-one.
2010-09-04
4-Chloro-N-[(E)-(3,4-dimeth-oxy-phen-yl)methyl-idene]aniline.
2010-08-18
(2E)-3-(3,4-Dimeth-oxy-phen-yl)-1-(2,5-dimethyl-thio-phen-3-yl)prop-2-en-1-one.
2010-07-31
Photoenhanced degradation of veratraldehyde upon the heterogeneous ozone reactions.
2010-07-21
2',3,4,4'-Tetra-meth-oxy-chalcone.
2010-06-26
Dimethyl 4-(3,4-dimethoxy-phen-yl)-2,6-dimethyl-1,4-dihydro-pyridine-3,5-dicarboxyl-ate.
2010-05-15
Racemization-free synthesis of (S)-(+)-tylophorine from L-proline by radical cyclization.
2010-05-07
Inhibition of Escherichia coli glycosyltransferase MurG and Mycobacterium tuberculosis Gal transferase by uridine-linked transition state mimics.
2010-04-01
Oxidative cleavage of diverse ethers by an extracellular fungal peroxygenase.
2009-10-23
(E)-N'-(3,4-Dimethoxy-benzyl-idene)-2,4-dihydroxy-benzohydrazide methanol solvate.
2009-09-09
Methyl 5,6-dimeth-oxy-1H-indole-2-carboxyl-ate.
2009-09-05
Tumor-specific cytotoxic activity of 1,2,3,4-tetrahydroisoquinoline derivatives against human oral squamous cell carcinoma cell lines.
2009-08
N,N'-Bis(3,4-dimethoxy-benzyl-idene)butane-1,4-diamine.
2009-07-04
Diisopropyl 3-[(E)-2-(3,4-dimethoxy-phen-yl)ethen-yl]-5-oxocyclo-hex-3-ene-1,1-dicarboxyl-ate.
2009-05-07
3-(3,4-Dimethoxy-phenyl)-1-(3-pyridyl)prop-2-en-1-one monohydrate.
2009-04-18
The total synthesis of fukiic acid, an HIV-1 integrase inhibitor.
2008-10
A validated reverse-phase HPLC analytical method for the quantification of phenolic compounds in Baccharis dracunculifolia.
2008-08-30
(E)-3-(3,4-Dimethoxy-phen-yl)-1-(2-thien-yl)prop-2-en-1-one.
2008-07-09
Determination of some aldehydes by using solid-phase microextraction and high-performance liquid chromatography with UV detection.
2008-01-16
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
A reliable quantitative method for the analysis of phenolic compounds in Brazilian propolis by reverse phase high performance liquid chromatography.
2007-11
A convenient allylsilane-N-acyliminium route toward indolizidine and quinolizidine alkaloids.
2007-10-02
Enhanced activity of strobilurin and fludioxonil by using berberine and phenolic compounds to target fungal antioxidative stress response.
2007-08
Combinatorial synthesis and characterization of new asymmetric porphyrins as potential photosensitizers in photodynamic therapy.
2007-07
Alpha-monodeuterated benzyl alcohols and phosphobetaines from reactions of aromatic aldehydes with a water/D2O-soluble phosphine.
2006-12-11
Targeting antioxidative signal transduction and stress response system: control of pathogenic Aspergillus with phenolics that inhibit mitochondrial function.
2006-07
Tetramethylammonium hydroxide (TMAH) thermochemolysis of lignin: behavior of 4-O-etherified cinnamyl alcohols and aldehydes.
2005-11-16
Asymmetric synthesis of tetrahydropalmatine via tandem 1,2-addition/cyclization.
2005-11-11
Involvement of lipid peroxidation in the degradation of a non-phenolic lignin model compound by manganese peroxidase of the litter-decomposing fungus Stropharia coronilla.
2005-05-06
Methyl jasmonate modulated biotransformation of phenylpropanoids to vanillin related metabolites using Capsicum frutescens root cultures.
2005-02
Identification of phenolics for control of Aspergillus flavus using Saccharomyces cerevisiae in a model target-gene bioassay.
2004-12-29
First synthesis of a polysaccharide-supported lignin model compound and study of its oxidation promoted by lignin peroxidase.
2004-01-02
Lignin peroxidase-catalyzed oxidation of nonphenolic trimeric lignin model compounds: fragmentation reactions in the intermediate radical cations.
2003-11-14
Mechanistic features of lignin peroxidase-catalyzed oxidation of substituted phenols and 1,2-dimethoxyarenes.
2003-10-10
Enzyme production by Mycena galopus mycelium in artificial media and in Picea sitchensis F1 horizon needle litter.
2003-08
Electroenzymatic oxidation of veratryl alcohol by lignin peroxidase.
2003-05-08
Isolation and characterization of aromatics-degrading microorganisms from the gut of the lower termite Coptotermes formosanus.
2003-04
Properties and functional significance of Saccharomyces cerevisiae ADHVI.
2003-02-01
[Dependence of activities of polysaccharide hydrolases and oxidases from Cerrena unicolor on the source of carbon and aromatic acids in culture media].
2002-06-19
Influence of aromatic compounds on biodegradation of [14C]-labeled xylan and mannan by the white-rot fungus Phlebia radiata.
2002-03
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.
2001-12
Antioxidant properties of 8.0.4'-neolignans.
2001-11
Characterization of aryl alcohol oxidase produced by dye-decolorizing fungus, Geotrichum candidum Decl.
2001
A new cyclobutane lignan from Cinnamomum balansae.
2001
Ligninolysis by a purified lignin peroxidase.
1993-06-15
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:38:23 GMT 2025
Edited
by admin
on Mon Mar 31 18:38:23 GMT 2025
Record UNII
UI88P68JZD
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
VERATRALDEHYDE
FCC   FHFI   MI  
Systematic Name English
VERAPAMIL RELATED COMPOUND E
USP-RS  
Preferred 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
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 Mon Mar 31 18:38:23 GMT 2025 , Edited by admin on Mon Mar 31 18:38:23 GMT 2025
CFR 21 CFR 172.515
Created by admin on Mon Mar 31 18:38:23 GMT 2025 , Edited by admin on Mon Mar 31 18:38:23 GMT 2025
Code System Code Type Description
JECFA MONOGRAPH
821
Created by admin on Mon Mar 31 18:38:23 GMT 2025 , Edited by admin on Mon Mar 31 18:38:23 GMT 2025
PRIMARY
RS_ITEM_NUM
1711439
Created by admin on Mon Mar 31 18:38:23 GMT 2025 , Edited by admin on Mon Mar 31 18:38:23 GMT 2025
PRIMARY
CHEBI
17098
Created by admin on Mon Mar 31 18:38:23 GMT 2025 , Edited by admin on Mon Mar 31 18:38:23 GMT 2025
PRIMARY
MERCK INDEX
m11415
Created by admin on Mon Mar 31 18:38:23 GMT 2025 , Edited by admin on Mon Mar 31 18:38:23 GMT 2025
PRIMARY Merck Index
FDA UNII
UI88P68JZD
Created by admin on Mon Mar 31 18:38:23 GMT 2025 , Edited by admin on Mon Mar 31 18:38:23 GMT 2025
PRIMARY
PUBCHEM
8419
Created by admin on Mon Mar 31 18:38:23 GMT 2025 , Edited by admin on Mon Mar 31 18:38:23 GMT 2025
PRIMARY
ECHA (EC/EINECS)
204-373-2
Created by admin on Mon Mar 31 18:38:23 GMT 2025 , Edited by admin on Mon Mar 31 18:38:23 GMT 2025
PRIMARY
SMS_ID
300000032738
Created by admin on Mon Mar 31 18:38:23 GMT 2025 , Edited by admin on Mon Mar 31 18:38:23 GMT 2025
PRIMARY
CAS
120-14-9
Created by admin on Mon Mar 31 18:38:23 GMT 2025 , Edited by admin on Mon Mar 31 18:38:23 GMT 2025
PRIMARY
NSC
8500
Created by admin on Mon Mar 31 18:38:23 GMT 2025 , Edited by admin on Mon Mar 31 18:38:23 GMT 2025
PRIMARY
NSC
24521
Created by admin on Mon Mar 31 18:38:23 GMT 2025 , Edited by admin on Mon Mar 31 18:38:23 GMT 2025
PRIMARY
WIKIPEDIA
VERATRALDEHYDE
Created by admin on Mon Mar 31 18:38:23 GMT 2025 , Edited by admin on Mon Mar 31 18:38:23 GMT 2025
PRIMARY
EPA CompTox
DTXSID7026285
Created by admin on Mon Mar 31 18:38:23 GMT 2025 , Edited by admin on Mon Mar 31 18:38:23 GMT 2025
PRIMARY
Related Record Type Details
PARENT -> IMPURITY
CHROMATOGRAPHIC PURITY (HPLC/UV)
EP