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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 DIOXOLANE

SMILES

C1COCO1

InChI

InChIKey=WNXJIVFYUVYPPR-UHFFFAOYSA-N
InChI=1S/C3H6O2/c1-2-5-3-4-1/h1-3H2

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
Stereocontrol of intramolecular Diels-Alder reactions: synthetic studies and transition structure modeling with c5-substituted 1,3,8-nonatrienes and nonadienynes.
2001 Jun 1
Simultaneous discrimination of diastereotopic groups and faces: the first example in intramolecular [3+2] and [2+2+1] cycloaddition reactions.
2001 Jun 1
The conformational origin of the barrier to the formation of neighboring group assistance in glycosylation reactions: a dynamical density functional theory study.
2001 Jun 13
Alkynoates as a source of reactive alkylinides for aldehyde addition reactions.
2001 Jun 14
A simple and versatile method for the synthesis of acetals from aldehydes and ketones using bismuth triflate.
2002 Jul 26
Orthoesters versus 2-O-acyl glycosides as glycosyl donors: theorectical and experimental studies.
2003 Oct 6
Fine-tuning monophosphine ligands for enhanced enantioselectivity. Influence of chiral hemilabile pendant groups.
2004 Apr 29
Structural chemistry of new lithium bis(oxalato)borate solvates.
2004 Dec
Electrolytic partial fluorination of organic compounds.71. Highly diastereoselective anodic fluorination of sulfides having oxygen-containing heterocyclic groups.
2004 Feb 20
Synthesis and biological activities of novel triazole compounds containing 1,3-dioxolane rings.
2004 Nov 30
Determination of 3-chloropropane-1,2-diol as its 1,3-dioxolane derivative at the microg kg-1 level: application to a wide range of foods.
2005 Dec
Rapid analysis of tile industry gaseous emissions by ion mobility spectrometry and comparison with solid phase micro-extraction/gas chromatography/mass spectrometry.
2006 Dec
Synthesis and anti-HSV-1 activity of quinolonic acyclovir analogues.
2006 Feb 15
Reactivity of fullerene epoxide: preparation of fullerene-fused thiirane, tetrahydrothiazolidin-2-one, and 1,3-dioxolane.
2008 Apr 4
Synthesis of uracil nucleotide analogs with a modified, acyclic ribose moiety as P2Y(2) receptor antagonists.
2009 Jul 15
Linking microscopic guest properties to macroscopic observables in clathrate hydrates: guest-host hydrogen bonding.
2009 May 7
Recent advances in synthetic bioelastomers.
2009 Nov 20
Synthesis and X-ray structure of a C5-C4-linked glucofuranose-oxazolidin-2-one.
2009 Oct 12
A systematic study on the activation of simple polyethers by MoCl5 and WCl6.
2010 Jun 14
Intrinsic acidity and electrophilicity of gaseous propargyl/allenyl carbocations.
2010 Jun 7
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 17:12:33 GMT 2023
Edited
by admin
on Fri Dec 15 17:12:33 GMT 2023
Record UNII
Y57RBG19JL
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIOXOLANE
INCI  
INCI  
Official Name English
ELCOTAL DX
Brand Name English
1,3-DIOXACYCLOPENTANE
Systematic Name English
1,3-DIOXOLANE [HSDB]
Common Name English
GLYCOLFORMAL
Common Name English
1,3-DIOXOLANE
HSDB  
Systematic Name English
1,3-DIOXOLAN
Systematic Name English
ETHYLENE GLYCOL FORMAL
Common Name English
FORMAL GLYCOL
Common Name English
5-CROWN-2
Common Name English
DIOXOLANE [INCI]
Common Name English
DIOXOLANE, 1,3-
Systematic Name English
Code System Code Type Description
WIKIPEDIA
DIOXOLANE
Created by admin on Fri Dec 15 17:12:33 GMT 2023 , Edited by admin on Fri Dec 15 17:12:33 GMT 2023
PRIMARY
MESH
C010962
Created by admin on Fri Dec 15 17:12:33 GMT 2023 , Edited by admin on Fri Dec 15 17:12:33 GMT 2023
PRIMARY
PUBCHEM
12586
Created by admin on Fri Dec 15 17:12:33 GMT 2023 , Edited by admin on Fri Dec 15 17:12:33 GMT 2023
PRIMARY
ECHA (EC/EINECS)
211-463-5
Created by admin on Fri Dec 15 17:12:33 GMT 2023 , Edited by admin on Fri Dec 15 17:12:33 GMT 2023
PRIMARY
RXCUI
2383339
Created by admin on Fri Dec 15 17:12:33 GMT 2023 , Edited by admin on Fri Dec 15 17:12:33 GMT 2023
PRIMARY
EPA CompTox
DTXSID4027284
Created by admin on Fri Dec 15 17:12:33 GMT 2023 , Edited by admin on Fri Dec 15 17:12:33 GMT 2023
PRIMARY
CHEBI
87597
Created by admin on Fri Dec 15 17:12:33 GMT 2023 , Edited by admin on Fri Dec 15 17:12:33 GMT 2023
PRIMARY
FDA UNII
Y57RBG19JL
Created by admin on Fri Dec 15 17:12:33 GMT 2023 , Edited by admin on Fri Dec 15 17:12:33 GMT 2023
PRIMARY
DAILYMED
Y57RBG19JL
Created by admin on Fri Dec 15 17:12:33 GMT 2023 , Edited by admin on Fri Dec 15 17:12:33 GMT 2023
PRIMARY
CAS
646-06-0
Created by admin on Fri Dec 15 17:12:33 GMT 2023 , Edited by admin on Fri Dec 15 17:12:33 GMT 2023
PRIMARY
HSDB
5737
Created by admin on Fri Dec 15 17:12:33 GMT 2023 , Edited by admin on Fri Dec 15 17:12:33 GMT 2023
PRIMARY