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Details

Stereochemistry ACHIRAL
Molecular Formula C2H6O2
Molecular Weight 62.0678
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of METHOXYMETHANOL

SMILES

COCO

InChI

InChIKey=VHWYCFISAQVCCP-UHFFFAOYSA-N
InChI=1S/C2H6O2/c1-4-2-3/h3H,2H2,1H3

HIDE SMILES / InChI

Molecular Formula C2H6O2
Molecular Weight 62.0678
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
2,2'-Bis(meth-oxy-meth-oxy)-3,3'-diphenyl-1,1'-binaphthalene.
2010-12-24
Mechanism and branching ratios of hydroxy ethers + (*)OH gas phase reactions: relevance of h bond interactions.
2010-07-22
Methanol as a reaction medium and reagent in substrate reactions of rhodium porphyrins.
2009-09-07
Di-tert-butyl N-[2,6-bis-(methoxy-meth-oxy)phen-yl]imino-diacetate.
2009-03-25
Ab initio study of substituent effects in the interactions of dimethyl ether with aromatic rings.
2008-05-21
2-(Methoxy-meth-oxy)-1-(4-oxobicyclo-[3.1.0]hexan-1-yl)ethyl 4-nitro-benzoate.
2007-12-21
Selective oxidation of methanol and ethanol on supported ruthenium oxide clusters at low temperatures.
2005-02-17
The irrationality of the present use of the osmole gap: applicable physical chemistry principles and recommendations to improve the validity of current practices.
2004
The use of the osmole gap as a screening test for the presence of exogenous substances.
2004
Diastereoselective photochromism of a bisbenzothienylethene governed by steric as well as electronic interactions.
2003-06-18
Synthesis and insecticidal activity of novel N-oxydihydropyrrole derivatives with a substituted spirocyclohexyl group.
2003-06
Proton-coupled electron transfer versus hydrogen atom transfer in benzyl/toluene, methoxyl/methanol, and phenoxyl/phenol self-exchange reactions.
2002-09-18
Diastereoselective reactions of delta-oxy-substituted allylic acetates with organocopper reagents.
2002-05-03
Substance Class Chemical
Created
by admin
on Mon Mar 31 19:06:29 GMT 2025
Edited
by admin
on Mon Mar 31 19:06:29 GMT 2025
Record UNII
9T7K15960E
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
FORMALDEHYDE METHYL HEMIACETAL
Preferred Name English
METHOXYMETHANOL
Systematic Name English
METHYLENE GLYCOL MONOMETHYL ETHER
Systematic Name English
METHANOL, METHOXY-
Systematic Name English
METHANOL HEMIFORMAL
Systematic Name English
METHANOL, 1-METHOXY-
Systematic Name English
HEMIFORMAL
Systematic Name English
METHYL HEMIFORMAL
Systematic Name English
Code System Code Type Description
EPA CompTox
DTXSID4027571
Created by admin on Mon Mar 31 19:06:29 GMT 2025 , Edited by admin on Mon Mar 31 19:06:29 GMT 2025
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FDA UNII
9T7K15960E
Created by admin on Mon Mar 31 19:06:29 GMT 2025 , Edited by admin on Mon Mar 31 19:06:29 GMT 2025
PRIMARY
WIKIPEDIA
Methoxymethanol
Created by admin on Mon Mar 31 19:06:29 GMT 2025 , Edited by admin on Mon Mar 31 19:06:29 GMT 2025
PRIMARY
CAS
4461-52-3
Created by admin on Mon Mar 31 19:06:29 GMT 2025 , Edited by admin on Mon Mar 31 19:06:29 GMT 2025
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CHEBI
46791
Created by admin on Mon Mar 31 19:06:29 GMT 2025 , Edited by admin on Mon Mar 31 19:06:29 GMT 2025
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PUBCHEM
62540
Created by admin on Mon Mar 31 19:06:29 GMT 2025 , Edited by admin on Mon Mar 31 19:06:29 GMT 2025
PRIMARY
ECHA (EC/EINECS)
224-722-2
Created by admin on Mon Mar 31 19:06:29 GMT 2025 , Edited by admin on Mon Mar 31 19:06:29 GMT 2025
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