VERATRALDEHYDE

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 Search

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

Title	Date	PubMed
Characterization of aryl alcohol oxidase produced by dye-decolorizing fungus, Geotrichum candidum Decl.	2001	16232969
A new cyclobutane lignan from Cinnamomum balansae.	2001	11841117
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	11802654
Dopamine D(3) receptor antagonists. 1. Synthesis and structure-activity relationships of 5,6-dimethoxy-N-alkyl- and N-alkylaryl-substituted 2-aminoindans.	2001 Dec 20	11741489
Characterization of the Saccharomyces cerevisiae YMR318C (ADH6) gene product as a broad specificity NADPH-dependent alcohol dehydrogenase: relevance in aldehyde reduction.	2002 Jan 1	11742541
Influence of aromatic compounds on biodegradation of [14C]-labeled xylan and mannan by the white-rot fungus Phlebia radiata.	2002 Mar	12074091
[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	12068574
Enzyme production by Mycena galopus mycelium in artificial media and in Picea sitchensis F1 horizon needle litter.	2003 Aug	14531622
Properties and functional significance of Saccharomyces cerevisiae ADHVI.	2003 Feb 1	12604208
Electroenzymatic oxidation of veratryl alcohol by lignin peroxidase.	2003 May 8	12730009
Lignin peroxidase-catalyzed oxidation of nonphenolic trimeric lignin model compounds: fragmentation reactions in the intermediate radical cations.	2003 Nov 14	14604381
Identification of phenolics for control of Aspergillus flavus using Saccharomyces cerevisiae in a model target-gene bioassay.	2004 Dec 29	15612761
First synthesis of a polysaccharide-supported lignin model compound and study of its oxidation promoted by lignin peroxidase.	2004 Jan 2	14672691
Methyl jasmonate modulated biotransformation of phenylpropanoids to vanillin related metabolites using Capsicum frutescens root cultures.	2005 Feb	15820659
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	15796893
Asymmetric synthesis of tetrahydropalmatine via tandem 1,2-addition/cyclization.	2005 Nov 11	16268624
Targeting antioxidative signal transduction and stress response system: control of pathogenic Aspergillus with phenolics that inhibit mitochondrial function.	2006 Jul	16834605
Combinatorial synthesis and characterization of new asymmetric porphyrins as potential photosensitizers in photodynamic therapy.	2007 Jul	17896942
A reliable quantitative method for the analysis of phenolic compounds in Brazilian propolis by reverse phase high performance liquid chromatography.	2007 Nov	17880032
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	18320020
(E)-3-(3,4-Dimethoxy-phen-yl)-1-(2-thien-yl)prop-2-en-1-one.	2008 Jul 9	21203155
Diisopropyl 3-[(E)-2-(3,4-dimethoxy-phen-yl)ethen-yl]-5-oxocyclo-hex-3-ene-1,1-dicarboxyl-ate.	2009 May 7	21583057
Methyl 5,6-dimeth-oxy-1H-indole-2-carboxyl-ate.	2009 Sep 5	21577822
Inhibition of Escherichia coli glycosyltransferase MurG and Mycobacterium tuberculosis Gal transferase by uridine-linked transition state mimics.	2010 Apr 1	20226679
4-Chloro-N-[(E)-(3,4-dimeth-oxy-phen-yl)methyl-idene]aniline.	2010 Aug 18	21588697
N'-(3,4-Dimeth-oxy-benzyl-idene)benzo-hydrazide.	2010 Dec 18	21522678
Photoenhanced degradation of veratraldehyde upon the heterogeneous ozone reactions.	2010 Jul 21	20502834
(2E)-3-(3,4-Dimeth-oxy-phen-yl)-1-(2,5-dimethyl-thio-phen-3-yl)prop-2-en-1-one.	2010 Jul 31	21588422
Racemization-free synthesis of (S)-(+)-tylophorine from L-proline by radical cyclization.	2010 May 7	20377275
(E)-3,5-Dimeth-oxy-benzaldehyde oxime.	2010 Oct 2	21588931
Parameters of Reserpine Analogs That Induce MSH2/MSH6-Dependent Cytotoxic Response.	2010 Sep 13	20936178
(E)-1-(2,5-Dichloro-3-thien-yl)-3-(3,4-dimeth-oxy-phen-yl)prop-2-en-1-one.	2010 Sep 4	21587480
Enhanced activity of antifungal drugs using natural phenolics against yeast strains of Candida and Cryptococcus.	2011 May	21332761

Patents

Substance Class	Chemical Created by `admin` on `Fri Dec 15 16:57:17 UTC 2023` Edited by `admin` on `Fri Dec 15 16:57:17 UTC 2023`
Record UNII	UI88P68JZD
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

VERATRALDEHYDE

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

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