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Details

Stereochemistry ACHIRAL
Molecular Formula C8H8O2
Molecular Weight 136.1479
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 3-METHOXYBENZALDEHYDE

SMILES

COC1=CC(C=O)=CC=C1

InChI

InChIKey=WMPDAIZRQDCGFH-UHFFFAOYSA-N
InChI=1S/C8H8O2/c1-10-8-4-2-3-7(5-8)6-9/h2-6H,1H3

HIDE SMILES / InChI

Molecular Formula C8H8O2
Molecular Weight 136.1479
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Aerosolized essential oils and individual natural product compounds as brown treesnake repellents.
2002 Aug
A novel potato defence-related alcohol:NADP+ oxidoreductase induced in response to Erwinia carotovora.
2003 May
Structure-function analysis of the vanillin molecule and its antifungal properties.
2005 Mar 9
Two novel series of allocolchicinoids with modified seven membered B-rings: design, synthesis, inhibition of tubulin assembly and cytotoxicity.
2005 May 16
Fumigant activity of plant essential oils and components from horseradish (Armoracia rusticana), anise (Pimpinella anisum) and garlic (Allium sativum) oils against Lycoriella ingenua (Diptera: Sciaridae).
2006 Aug
Effect of natural phenol derivatives on skeletal type sarcoplasmic reticulum Ca2+ -ATPase and ryanodine receptor.
2007
Equilibrium and kinetic studies for the sorption of 3-methoxybenzaldehyde on activated kaolinites.
2007 Mar 6
N,N'-Bis(3-methoxy-benzyl-idene)ethane-1,2-diamine.
2008 Aug 23
N-[4-Acetyl-5-(3-methoxy-phen-yl)-4,5-dihydro-1,3,4-thia-diazol-2-yl]acetamide.
2008 Oct 11
(4S,5S)-2-(3-Methoxy-phen-yl)-1,3-dioxolane-4,5-dicarboxamide.
2009 Aug 26
2-(3,5-Di-tert-butyl-4-hydroxy-benzyl-sulfan-yl)-N'-(3-methoxy-benzyl-idene)acetohydrazide.
2009 Aug 8
1-(6-Chloro-2-methyl-4-phenyl-quinolin-3-yl)-3-(3-methoxy-phen-yl)prop-2-en-1-one.
2009 Dec 9
2-Methoxy-benzaldehyde 2,4-dinitro-phenyl-hydrazone.
2009 Jan 8
4-Chloro-N'-(2-methoxy-benzyl-idene)benzohydrazide.
2009 Mar 25
3-Methoxy-benzaldehyde thio-semi-carbazone.
2009 Mar 28
A synthetic approach of new trans-substituted hydroxylporphyrins.
2010
2-(3,4-Dimethyl-5,5-dioxo-2H,4H-pyrazolo-[4,3-c][1,2]benzothia-zin-2-yl)-N'-(3-meth-oxy-benzyl-idene)aceto-hydrazide dimethyl-formamide hemisolvate.
2010 Dec 24
Ethyl (2Z)-2-(3-methoxy-benzyl-idene)-7-methyl-3-oxo-5-phenyl-2,3-dihydro-5H-1,3-thia-zolo[3,2-a]pyrimidine-6-carboxyl-ate.
2010 Feb 13
Parameters of Reserpine Analogs That Induce MSH2/MSH6-Dependent Cytotoxic Response.
2010 Sep 13
Interesting anticandidal effects of anisic aldehydes on growth and proton-pumping-ATPase-targeted activity.
2011 Oct
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:15:20 GMT 2023
Edited
by admin
on Fri Dec 15 17:15:20 GMT 2023
Record UNII
8ZAO7S0IVH
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3-METHOXYBENZALDEHYDE
Systematic Name English
METAMETHOXYBENZALDEHYDE
Systematic Name English
3-METHOXYPHENYLCARBOXALDEHYDE
Common Name English
ANISALDEHYDE, M-
Systematic Name English
BENZALDEHYDE, 3-METHOXY-
Systematic Name English
M-ANISALDEHYDE
Systematic Name English
M-METHOXYBENZALDEHYDE
Systematic Name English
NSC-43794
Code English
BENZALDEHYDE, M-METHOXY-
Systematic Name English
Code System Code Type Description
CHEBI
136805
Created by admin on Fri Dec 15 17:15:20 GMT 2023 , Edited by admin on Fri Dec 15 17:15:20 GMT 2023
PRIMARY
ECHA (EC/EINECS)
209-712-8
Created by admin on Fri Dec 15 17:15:20 GMT 2023 , Edited by admin on Fri Dec 15 17:15:20 GMT 2023
PRIMARY
NSC
43794
Created by admin on Fri Dec 15 17:15:20 GMT 2023 , Edited by admin on Fri Dec 15 17:15:20 GMT 2023
PRIMARY
PUBCHEM
11569
Created by admin on Fri Dec 15 17:15:20 GMT 2023 , Edited by admin on Fri Dec 15 17:15:20 GMT 2023
PRIMARY
CAS
591-31-1
Created by admin on Fri Dec 15 17:15:20 GMT 2023 , Edited by admin on Fri Dec 15 17:15:20 GMT 2023
PRIMARY
FDA UNII
8ZAO7S0IVH
Created by admin on Fri Dec 15 17:15:20 GMT 2023 , Edited by admin on Fri Dec 15 17:15:20 GMT 2023
PRIMARY
EPA CompTox
DTXSID5044447
Created by admin on Fri Dec 15 17:15:20 GMT 2023 , Edited by admin on Fri Dec 15 17:15:20 GMT 2023
PRIMARY