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

Details

Stereochemistry ACHIRAL
Molecular Formula C4H8O2
Molecular Weight 88.1051
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of 1,3-DIOXANE

SMILES

C1COCOC1

InChI

InChIKey=VDFVNEFVBPFDSB-UHFFFAOYSA-N
InChI=1S/C4H8O2/c1-2-5-4-6-3-1/h1-4H2

HIDE SMILES / InChI

Molecular Formula C4H8O2
Molecular Weight 88.1051
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Product study of the OH radical and Cl atom initiated oxidation of 1,3-dioxane.
2010-12-17
3,9-Di-tert-butyl-2,4,8,10-tetra-oxaspiro-[5.5]undeca-ne.
2010-11-30
Stereoselective α,α'-annelation reactions of 1,3-dioxan-5-ones.
2010-11-05
3,3,9,9-Tetra-phenyl-2,4,8,10-tetra-oxa-spiro-[5.5]undeca-ne.
2010-10-31
3-(4-Meth-oxy-benzyl-idene)-1,5-dioxa-spiro-[5.5]undecane-2,4-dione.
2010-10-20
Synthesis and characterization of novel indole derivatives reveal improved therapeutic agents for treatment of ischemia/reperfusion (I/R) injury.
2010-09-23
5-(4-Fluoro-benzyl-idene)-2,2-dimethyl-1,3-dioxane-4,6-dione.
2010-08-21
(E)-1-[(1,3-Dioxan-4-yl)meth-yl]-2-(nitro-methyl-idene)imidazolidine.
2010-08-21
5-(4-Hy-droxy-benzyl-idene)-2,2-dimethyl-1,3-dioxane-4,6-dione.
2010-08-18
3,9-Bis(2,4-dichloro-phen-yl)-2,4,8,10-tetra-oxaspiro-[5.5]undeca-ne.
2010-06-30
Xyloccensin e.
2010-05-15
3,9-Di-1-naphthyl-2,4,8,10-tetra-oxa-spiro-[5.5]undeca-ne.
2010-04-28
Bifunctional hydrogen bonds in monohydrated cycloether complexes.
2010-03-04
2-(2-Naphth-yl)-1,3-dioxane.
2010-01-30
3,9-Bis(2-chloro-phen-yl)-2,4,8,10-tetra-oxaspiro-[5.5]undeca-ne.
2010-01-23
Synthetic mRNA splicing modulator compounds with in vivo antitumor activity.
2009-11-26
2-(2-Nitro-phen-yl)-1,3-dioxan-5-ol.
2009-10-28
5-(2-Fluoro-benzyl-idene)-2,2-dimethyl-1,3-dioxane-4,6-dione.
2009-09-30
(Z)-3-(3-Phenyl-allyl-idene)-1,5-dioxa-spiro-[5.5]undecane-2,4-dione.
2009-09-30
3-[(5-Methyl-furan-2-yl)methyl-ene]-1,5-dioxaspiro-[5.5]undecane-2,4-dione.
2009-07-29
3-(2-Furylmethyl-ene)-1,5-dioxaspiro-[5.5]undecane-2,4-dione.
2009-07-15
Synthesis of uracil nucleotide analogs with a modified, acyclic ribose moiety as P2Y(2) receptor antagonists.
2009-07-15
Biodegradation of 1,4-dioxane and transformation of related cyclic compounds by a newly isolated Mycobacterium sp. PH-06.
2009-07
7,14-Bis(4-bromo-phen-yl)-2,11,11-trimethyl-1,4,10,12-tetra-oxa-dispiro-[4.2.5.2]penta-decane-9,13-dione.
2009-04-30
7,14-Bis(4-methoxy-phen-yl)-11,11-dimethyl-1,4,10,12-tetra-oxa-dispiro-[4.2.5.2]penta-decane-9,13-dione.
2009-04-18
2,3:4,6-Di-O-isopropylidene-alpha-L-sorbofuranose and 2,3-O-isopropylidene-alpha-L-sorbofuranose.
2009-04
2,2-Dimethyl-5-triphenyl-methyl-1,3-dioxane.
2009-01-14
Reactivity of 13,13-dibromo-2,4,9,11-tetraoxadispiro[5.0.5.1]tridecane toward organolithiums: remarkable resistance to the DMS rearrangement.
2008-08-01
5,5-Bis(hydroxy-meth-yl)-2-phenyl-1,3-dioxane.
2008-07-19
Synthesis of polynucleotide analogs containing a polyvinyl alcohol backbone.
2008-03-26
Sugar derived hexacoordinated phosphates: chiral anionic auxiliaries with general asymmetric efficiency.
2008-03
New 1,3-dioxolane and 1,3-dioxane derivatives as effective modulators to overcome multidrug resistance.
2007-03-15
Oxygenation vs iodonio substitution during the reactions of alkenyl-silanes with iodosylbenzene: participation of the internal oxy group.
2007-03-12
Ambient-pressure organic superconductors kappa-(DMEDO-TSeF)2[Au(CN)4](solv.): Tc tuning by modification of the solvent of crystallization.
2007
Photoreactions in the gas-phase complexes of Mg(*+)-dioxanes.
2006-04-06
Relationships between the structure of dexoxadrol and etoxadrol analogues and their NMDA receptor affinity.
2006
Hybrid density functional theory study of fragment ions generated during mass spectrometry of 1,3-dioxane derivatives.
2006
Conformational pathways of saturated six-membered rings. A static and dynamical density functional study.
2005-09-15
Modular synthesis and preliminary biological evaluation of stereochemically diverse 1,3-dioxanes.
2004-09
Modeling deoxyribose radicals by neutralization-reionization mass spectrometry. Part 1. Preparation, dissociations, and energetics of 2-hydroxyoxolan-2-yl radical, neutral isomers, and cations.
2004-07
Design and synthesis of new macrocyclic cyclophanes using 1,3-dioxane units as bridges: a molecular "rocking chair".
2004-02-20
Synthesis and NMDA-receptor affinity of ring and side chain homologous dexoxadrol derivatives.
2004-02
Exclusive formation of alpha-methyleneoxetanes in ketene-alkene cycloadditions. Evidence for intervention of both an alpha-methyleneoxetane and the subsequent 1,4-zwitterion.
2003-11-26
Palladium-catalyzed Heck reaction on 1-alkoxy-1,3-dienes: a regioselective gamma-arylation of alpha,beta-unsaturated carbonyl compounds.
2003-10-16
Structural biasing elements for in-cell histone deacetylase paralog selectivity.
2003-05-14
Synthesis of a novel series of tricyclic indan derivatives as melatonin receptor agonists.
2002-09-12
Effect of geminal substitution on the strain energy of dioxiranes. Origin of the low ring strain of dimethyldioxirane.
2002-05-31
Synthesis and biological activity of 1-phenylsulfonyl-4-phenylsulfonylaminopyrrolidine derivatives as thromboxane a(2) receptor antagonists.
2002-05
Can the stereochemical outcome of glycosylation reactions be controlled by the conformational preferences of the glycosyl donor?
2002-04-17
Diastereoselective synthesis of protected syn 1,3-diols: preparation of the C16-C24 portion of Dolabelides.
2002-02-07
Substance Class Chemical
Created
by admin
on Mon Mar 31 18:42:11 GMT 2025
Edited
by admin
on Mon Mar 31 18:42:11 GMT 2025
Record UNII
B2C8M17I09
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
1,3-DIOXANE
HSDB  
Systematic Name English
NSC-139436
Preferred Name English
1,3-PROPANEDIOL FORMAL
Common Name English
1,3-DIOXANE [HSDB]
Common Name English
M-DIOXIN, DIHYDRO-
Systematic Name English
TRIMETHYLENE GLYCOL METHYLENE ETHER
Common Name English
1,3-DIOXACYCLOHEXANE
Systematic Name English
M-DIOXANE
Systematic Name English
Code System Code Type Description
FDA UNII
B2C8M17I09
Created by admin on Mon Mar 31 18:42:11 GMT 2025 , Edited by admin on Mon Mar 31 18:42:11 GMT 2025
PRIMARY
CHEBI
46924
Created by admin on Mon Mar 31 18:42:11 GMT 2025 , Edited by admin on Mon Mar 31 18:42:11 GMT 2025
PRIMARY
NSC
139436
Created by admin on Mon Mar 31 18:42:11 GMT 2025 , Edited by admin on Mon Mar 31 18:42:11 GMT 2025
PRIMARY
EPA CompTox
DTXSID3025174
Created by admin on Mon Mar 31 18:42:11 GMT 2025 , Edited by admin on Mon Mar 31 18:42:11 GMT 2025
PRIMARY
ECHA (EC/EINECS)
208-005-1
Created by admin on Mon Mar 31 18:42:11 GMT 2025 , Edited by admin on Mon Mar 31 18:42:11 GMT 2025
PRIMARY
PUBCHEM
10450
Created by admin on Mon Mar 31 18:42:11 GMT 2025 , Edited by admin on Mon Mar 31 18:42:11 GMT 2025
PRIMARY
CAS
505-22-6
Created by admin on Mon Mar 31 18:42:11 GMT 2025 , Edited by admin on Mon Mar 31 18:42:11 GMT 2025
PRIMARY
HSDB
4263
Created by admin on Mon Mar 31 18:42:11 GMT 2025 , Edited by admin on Mon Mar 31 18:42:11 GMT 2025
PRIMARY
WIKIPEDIA
1,3-Dioxane
Created by admin on Mon Mar 31 18:42:11 GMT 2025 , Edited by admin on Mon Mar 31 18:42:11 GMT 2025
PRIMARY