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

Details

Stereochemistry ACHIRAL
Molecular Formula C3H6O2
Molecular Weight 74.0785
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of METHOXYACETALDEHYDE

SMILES

COCC=O

InChI

InChIKey=YSEFYOVWKJXNCH-UHFFFAOYSA-N
InChI=1S/C3H6O2/c1-5-3-2-4/h2H,3H2,1H3

HIDE SMILES / InChI

Molecular Formula C3H6O2
Molecular Weight 74.0785
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Recent N-atom containing compounds from indo-pacific invertebrates.
2010-11-10
Mitochondrial aldehyde dehydrogenase and cardiac diseases.
2010-10-01
Alcohol and acetaldehyde in public health: from marvel to menace.
2010-04
Human aldehyde dehydrogenase-catalyzed oxidation of ethylene glycol ether aldehydes.
2009-03-16
Methyl 2-(N-methoxy-carbonyl-meth-yl-N-methylsulfamo-yl)benzoate.
2009-02-04
Koshikamide B, a cytotoxic peptide lactone from a marine sponge Theonella sp.
2008-10-17
Methyl 2-{[(4-hydroxy-phen-yl)(methoxy-carbon-yl)meth-yl]amino-carbon-yl}ethano-ate hemihydrate.
2008-03-05
Salarins a and B and tulearin a: new cytotoxic sponge-derived macrolides.
2008-01-17
Azithromycin-sulfonamide conjugates as inhibitors of resistant Streptococcus pyogenes strains.
2007-02
Efficient enzymatic synthesis of phosphoroselenoate RNA by using adenosine 5'-(alpha-P-seleno)triphosphate.
2005-12-16
An inverse substrate orientation for the regioselective acylation of 3',5'-diaminonucleosides catalyzed by Candida antarctica lipase B?
2005-08
Proteomic identification of less oxidized brain proteins in aged senescence-accelerated mice following administration of antisense oligonucleotide directed at the Abeta region of amyloid precursor protein.
2005-07-29
Biotic and abiotic degradation behaviour of ethylene glycol monomethyl ether (EGME).
2005-05
Synthesis and fungicidal activity of new N,O-acyl chitosan derivatives.
2004-03-09
Gas chromatography-mass spectrometry of carbonyl compounds in cigarette mainstream smoke after derivatization with 2,4-dinitrophenylhydrazine.
2004-02-20
Oxidative generation of guanine radicals by carbonate radicals and their reactions with nitrogen dioxide to form site specific 5-guanidino-4-nitroimidazole lesions in oligodeoxynucleotides.
2003-08
Involvement of caspase 3 mediated apoptosis in hematopoietic cytotoxicity of metabolites of ethylene glycol monomethyl ether.
2002-10
High-throughput analysis of hemoglobin from neonates using matrix-assisted laser desorption/ionization time-of-flight mass spectrometry.
2002-06
Preparation, structure, and properties of a new giant manganese oxo-alkoxide wheel, [Mn19O12(OC2H4OCH3)14(HOC2H4OCH3)10]. HOC2H4OCH3.
2001-08-17
2-Methoxyethanol metabolism, embryonic distribution, and macromolecular adduct formation in the rat: the effect of radiofrequency radiation-induced hyperthermia.
2001-05-31
Immunochemical assay of hemoglobin with N(epsilon)-(carboxymethyl)lysine at lysine 66 of the beta chain.
2001
Apoptosis inhibition and ornithine decarboxylase superinduction as early epigenetic events in morphological transformation of Syrian hamster embryo cells exposed to 2-methoxyacetaldehyde, a metabolite of 2-methoxyethanol.
1999-03-29
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:36:58 GMT 2025
Edited
by admin
on Mon Mar 31 19:36:58 GMT 2025
Record UNII
5G4O7K64WA
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
METHOXYACETALDEHYDE
Systematic Name English
O-METHYLGLYCOLALDEHYDE
Preferred Name English
ACETALDEHYDE, METHOXY-
Systematic Name English
.ALPHA.-METHOXYACETALDEHYDE
Systematic Name English
2-METHOXYACETALDEHYDE
Systematic Name English
2-METHOXYETHANAL
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID90145651
Created by admin on Mon Mar 31 19:36:58 GMT 2025 , Edited by admin on Mon Mar 31 19:36:58 GMT 2025
PRIMARY
CAS
10312-83-1
Created by admin on Mon Mar 31 19:36:58 GMT 2025 , Edited by admin on Mon Mar 31 19:36:58 GMT 2025
PRIMARY
FDA UNII
5G4O7K64WA
Created by admin on Mon Mar 31 19:36:58 GMT 2025 , Edited by admin on Mon Mar 31 19:36:58 GMT 2025
PRIMARY
PUBCHEM
91563
Created by admin on Mon Mar 31 19:36:58 GMT 2025 , Edited by admin on Mon Mar 31 19:36:58 GMT 2025
PRIMARY
ECHA (EC/EINECS)
233-693-5
Created by admin on Mon Mar 31 19:36:58 GMT 2025 , Edited by admin on Mon Mar 31 19:36:58 GMT 2025
PRIMARY