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

Details

Stereochemistry ACHIRAL
Molecular Formula C5H10O3
Molecular Weight 118.1311
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of Ethyl carbonate

SMILES

CCOC(=O)OCC

InChI

InChIKey=OIFBSDVPJOWBCH-UHFFFAOYSA-N
InChI=1S/C5H10O3/c1-3-7-5(6)8-4-2/h3-4H2,1-2H3

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
Flowerlike vanadium sesquioxide: solvothermal preparation and electrochemical properties.
2010-10-25
Theoretical investigations on oxidative stability of solvents and oxidative decomposition mechanism of ethylene carbonate for lithium ion battery use.
2009-12-31
Diethyl 2,6-dimethyl-pyridine-3,5-dicarboxyl-ate at 100 K.
2009-09-26
Effects of solvents and salt on the thermal stability of lithiated graphite used in lithium ion battery.
2009-08-15
Effects of dimethyl or diethyl carbonate as an additive on volatility and flash point of an aviation fuel.
2009-01-30
Synthesis, structure, electrochemistry, and cytotoxic properties of ferrocenyl ester derivatives.
2009
Organic carbonates as alternative solvents for palladium-catalyzed substitution reactions.
2008
Synthesis of a new scaffold: the 7H,8H-pyrimido[1,6-b]pyridazin-6,8-dione nucleus.
2007-12-30
Diethyl 2-tert-butyl-6,9-dibromo-4,11-dioxo-5,10-dihydro-cis-1H,3H,4H,11H-2-azo-3a,4a,10a,11a-tetra-aza-benz[f]indeno[2,1,7-ija]azulene-11b,11c-dicarboxyl-ate.
2007-12-06
Preferential intramolecular ring closure of aminoalcohols with diethyl carbonate to oxazolidinones.
2007-05
Direct Yellow and Methylene Blue liquid-liquid extraction with alkylene carbonates.
2005-08
Solvent decompositions and physical properties of decomposition compounds in Li-ion battery electrolytes studied by DFT calculations and molecular dynamics simulations.
2005-02-24
Enzymatic synthesis and chemical recycling of poly(carbonate-urethane).
2004-08-09
Nucleophilic substitution reactions of aryl N-phenyl thiocarbamates with benzylamines in acetonitrile.
2004-04-30
An efficient synthesis of organic carbonates: atom economic protocol with a new catalytic system.
2004-03-21
[Product analysis of oxo synthesis of diethyl carbonate by GC/MS].
2004-03
Ion-molecule interactions in solutions of lithium perchlorate in propylene carbonate + diethyl carbonate mixtures: an IR and molecular orbital study.
2002-08
Steryl and stanyl esters of fatty acids by solvent-free esterification and transesterification in vacuo using lipases from Rhizomucor miehei, Candida antarctica, and Carica papaya.
2001-11
[An IR study of ion solvation and association of lithium perchlorate in some organic solvents].
2001-08
Comparison of pharmacophore cinnoline and quinoline systems on the basis of computer calculation and pharmacological screening of their condensed systems.
2001-06
Patents
Name Type Language
Ethyl carbonate
MI  
Systematic Name English
DIETHYL CARBONATE
HSDB  
Preferred Name English
CARBONIC ACID DIETHYL ESTER
Systematic Name English
ETHYL CARBONATE [MI]
Common Name English
NSC-8849
Code English
NCI-C60899
Code English
DIETHYL CARBONATE [HSDB]
Common Name English
Code System Code Type Description
MESH
C017858
Created by admin on Mon Mar 31 19:17:07 GMT 2025 , Edited by admin on Mon Mar 31 19:17:07 GMT 2025
PRIMARY
PUBCHEM
7766
Created by admin on Mon Mar 31 19:17:07 GMT 2025 , Edited by admin on Mon Mar 31 19:17:07 GMT 2025
PRIMARY
CAS
105-58-8
Created by admin on Mon Mar 31 19:17:07 GMT 2025 , Edited by admin on Mon Mar 31 19:17:07 GMT 2025
PRIMARY
MERCK INDEX
m5105
Created by admin on Mon Mar 31 19:17:07 GMT 2025 , Edited by admin on Mon Mar 31 19:17:07 GMT 2025
PRIMARY Merck Index
NSC
8849
Created by admin on Mon Mar 31 19:17:07 GMT 2025 , Edited by admin on Mon Mar 31 19:17:07 GMT 2025
PRIMARY
EPA CompTox
DTXSID3025041
Created by admin on Mon Mar 31 19:17:07 GMT 2025 , Edited by admin on Mon Mar 31 19:17:07 GMT 2025
PRIMARY
WIKIPEDIA
DIETHYL CARBONATE
Created by admin on Mon Mar 31 19:17:07 GMT 2025 , Edited by admin on Mon Mar 31 19:17:07 GMT 2025
PRIMARY
ECHA (EC/EINECS)
203-311-1
Created by admin on Mon Mar 31 19:17:07 GMT 2025 , Edited by admin on Mon Mar 31 19:17:07 GMT 2025
PRIMARY
CHEBI
50849
Created by admin on Mon Mar 31 19:17:07 GMT 2025 , Edited by admin on Mon Mar 31 19:17:07 GMT 2025
PRIMARY
FDA UNII
3UA92692HG
Created by admin on Mon Mar 31 19:17:07 GMT 2025 , Edited by admin on Mon Mar 31 19:17:07 GMT 2025
PRIMARY
HSDB
925
Created by admin on Mon Mar 31 19:17:07 GMT 2025 , Edited by admin on Mon Mar 31 19:17:07 GMT 2025
PRIMARY