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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
Interesting anticandidal effects of anisic aldehydes on growth and proton-pumping-ATPase-targeted activity.
2011-10
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.
2010-12-24
Parameters of Reserpine Analogs That Induce MSH2/MSH6-Dependent Cytotoxic Response.
2010-09-13
4-[3-(2H-Benzotriazol-2-yl)prop-oxy]-3-methoxy-benzaldehyde.
2010-05-08
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.
2010-02-13
9-(3-Methoxy-phen-yl)-6,6-dimethyl-4-phenyl-2,3,5,6,7,9-hexa-hydro-thieno[3,2-b]quinolin-8(4H)-one 1,1-dioxide.
2010-02-06
A synthetic approach of new trans-substituted hydroxylporphyrins.
2010
1-(6-Chloro-2-methyl-4-phenyl-quinolin-3-yl)-3-(3-methoxy-phen-yl)prop-2-en-1-one.
2009-12-09
(4S,5S)-2-(3-Methoxy-phen-yl)-1,3-dioxolane-4,5-dicarboxamide.
2009-08-26
2-(3,5-Di-tert-butyl-4-hydroxy-benzyl-sulfan-yl)-N'-(3-methoxy-benzyl-idene)acetohydrazide.
2009-08-08
3-Methoxy-benzaldehyde thio-semi-carbazone.
2009-03-28
4-Chloro-N'-(2-methoxy-benzyl-idene)benzohydrazide.
2009-03-25
2-Methoxy-benzaldehyde 2,4-dinitro-phenyl-hydrazone.
2009-01-08
N-[4-Acetyl-5-(3-methoxy-phen-yl)-4,5-dihydro-1,3,4-thia-diazol-2-yl]acetamide.
2008-10-11
N,N'-Bis(3-methoxy-benzyl-idene)ethane-1,2-diamine.
2008-08-23
Intramolecular charge transfer effects on 4-hydroxy-3-methoxybenzaldehyde.
2008-03
Characterization of ligV essential for catabolism of vanillin by Sphingomonas paucimobilis SYK-6.
2007-10
Equilibrium and kinetic studies for the sorption of 3-methoxybenzaldehyde on activated kaolinites.
2007-03-06
Effect of natural phenol derivatives on skeletal type sarcoplasmic reticulum Ca2+ -ATPase and ryanodine receptor.
2007
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).
2006-08
Two novel series of allocolchicinoids with modified seven membered B-rings: design, synthesis, inhibition of tubulin assembly and cytotoxicity.
2005-05-16
Structure-function analysis of the vanillin molecule and its antifungal properties.
2005-03-09
A novel potato defence-related alcohol:NADP+ oxidoreductase induced in response to Erwinia carotovora.
2003-05
Aerosolized essential oils and individual natural product compounds as brown treesnake repellents.
2002-08
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:42:58 GMT 2025
Edited
by admin
on Mon Mar 31 18:42:58 GMT 2025
Record UNII
8ZAO7S0IVH
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
3-METHOXYBENZALDEHYDE
Systematic Name English
NSC-43794
Preferred 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
BENZALDEHYDE, M-METHOXY-
Systematic Name English
Code System Code Type Description
CHEBI
136805
Created by admin on Mon Mar 31 18:42:58 GMT 2025 , Edited by admin on Mon Mar 31 18:42:58 GMT 2025
PRIMARY
ECHA (EC/EINECS)
209-712-8
Created by admin on Mon Mar 31 18:42:58 GMT 2025 , Edited by admin on Mon Mar 31 18:42:58 GMT 2025
PRIMARY
NSC
43794
Created by admin on Mon Mar 31 18:42:58 GMT 2025 , Edited by admin on Mon Mar 31 18:42:58 GMT 2025
PRIMARY
PUBCHEM
11569
Created by admin on Mon Mar 31 18:42:58 GMT 2025 , Edited by admin on Mon Mar 31 18:42:58 GMT 2025
PRIMARY
CAS
591-31-1
Created by admin on Mon Mar 31 18:42:58 GMT 2025 , Edited by admin on Mon Mar 31 18:42:58 GMT 2025
PRIMARY
FDA UNII
8ZAO7S0IVH
Created by admin on Mon Mar 31 18:42:58 GMT 2025 , Edited by admin on Mon Mar 31 18:42:58 GMT 2025
PRIMARY
EPA CompTox
DTXSID5044447
Created by admin on Mon Mar 31 18:42:58 GMT 2025 , Edited by admin on Mon Mar 31 18:42:58 GMT 2025
PRIMARY