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

Details

Stereochemistry ACHIRAL
Molecular Formula C6H10O4
Molecular Weight 146.1412
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIETHYL OXALATE

SMILES

CCOC(=O)C(=O)OCC

InChI

InChIKey=WYACBZDAHNBPPB-UHFFFAOYSA-N
InChI=1S/C6H10O4/c1-3-9-5(7)6(8)10-4-2/h3-4H2,1-2H3

HIDE SMILES / InChI

Molecular Formula C6H10O4
Molecular Weight 146.1412
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

Sourcing

Sourcing

Vendor/AggregatorIDURL
PubMed

PubMed

TitleDatePubMed
Efficient synthesis and hydrolysis of cyclic oxalate esters of glycols.
2002 Mar
Synthesis and quantitative structure-activity relationships of oxanilates as chemical hybridizing agents for wheat (Triticum aestivum L.).
2003 Feb 12
Identity double-proton transfer in (3Z)-3-hydroxy-1,4-di(quinolin-2-yl)but-3-en-2-one.
2003 Jun 16
A sensitive and robust method for obtaining intermolecular NOEs between side chains in large protein complexes.
2003 Mar
Template synthesis of Co(II), Ni(II) and Cu(II) complexes derived from oxamide ligand and the reactivity of Cu(II) complex towards human serum albumin.
2004
Antinociceptive activity of new imidazolidine carbonyl derivatives. Part 4. Synthesis and pharmacological activity of 8-aryl-3,4-dioxo-2H,8H-6,7-dihydroimidazo[2,1-c] [1,2,4]triazines.
2005 Feb
Spectroscopic approach in characterization of chromium(III), manganese(II), iron(III) and copper(II) complexes with a nitrogen donor tetradentate, 14-membered azamacrocyclic ligand.
2005 Jul
Synthesis, antibacterial, antifungal activity and interaction of CT-DNA with a new benzimidazole derived Cu(II) complex.
2005 Nov
Unambiguous synthesis and prophylactic antimalarial activities of imidazolidinedione derivatives.
2005 Oct 6
Synthesis of highly substituted enantiopure piperazines and ketopiperazines from vicinal N-sulfinyl diamines.
2006 Feb 17
Practical formal total synthesis of (rac)- and (S)-camptothecin.
2006 Feb 7
Ethyl 3-benzoyl-2-hydroxy-prop-2-enoate.
2007 Dec 6
Human immunodeficiency virus integrase inhibitors efficiently suppress feline immunodeficiency virus replication in vitro and provide a rationale to redesign antiretroviral treatment for feline AIDS.
2007 Oct 30
Conformational properties, chiroptical spectra, and molecular self-assembly of 2,3-piperazinodiones and their dithiono analogues.
2008 Apr 4
Novel quinolinonyl diketo acid derivatives as HIV-1 integrase inhibitors: design, synthesis, and biological activities.
2008 Aug 14
A new class of anticonvulsants possessing 6 Hz activity: 3,4-dialkyloxy thiophene bishydrazones.
2009 Nov
Synthesis and anticonvulsant activity of some new bishydrazones derived from 3,4-dipropyloxythiophene.
2009 Sep
Synthesis and biological activities of some novel triazoloquinazolines and triazinoquinazolines containing benzenesulfonamide moieties.
2010
(Z)-Ethyl 2-oxo-3-(1,2-dihydroquinolin-2-yl-idene)propano-ate.
2010 Jun 23
Patents
Substance Class Chemical
Created
by admin
on Fri Dec 15 15:22:05 GMT 2023
Edited
by admin
on Fri Dec 15 15:22:05 GMT 2023
Record UNII
860M3ZWF6J
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
DIETHYL OXALATE
HSDB   INCI   MI  
INCI  
Official Name English
NSC-8851
Code English
DIETHYL OXALATE [HSDB]
Common Name English
DIETHYL OXALATE [INCI]
Common Name English
ETHANEDIOC ACID, DIETHYL ESTER
Common Name English
DIETHYL OXALATE [MI]
Common Name English
ETHYL OXOLATE
Systematic Name English
Code System Code Type Description
CAS
95-92-1
Created by admin on Fri Dec 15 15:22:05 GMT 2023 , Edited by admin on Fri Dec 15 15:22:05 GMT 2023
PRIMARY
PUBCHEM
7268
Created by admin on Fri Dec 15 15:22:05 GMT 2023 , Edited by admin on Fri Dec 15 15:22:05 GMT 2023
PRIMARY
ECHA (EC/EINECS)
202-464-1
Created by admin on Fri Dec 15 15:22:05 GMT 2023 , Edited by admin on Fri Dec 15 15:22:05 GMT 2023
PRIMARY
MERCK INDEX
m4412
Created by admin on Fri Dec 15 15:22:05 GMT 2023 , Edited by admin on Fri Dec 15 15:22:05 GMT 2023
PRIMARY Merck Index
HSDB
2131
Created by admin on Fri Dec 15 15:22:05 GMT 2023 , Edited by admin on Fri Dec 15 15:22:05 GMT 2023
PRIMARY
FDA UNII
860M3ZWF6J
Created by admin on Fri Dec 15 15:22:05 GMT 2023 , Edited by admin on Fri Dec 15 15:22:05 GMT 2023
PRIMARY
NSC
8851
Created by admin on Fri Dec 15 15:22:05 GMT 2023 , Edited by admin on Fri Dec 15 15:22:05 GMT 2023
PRIMARY
EPA CompTox
DTXSID2044472
Created by admin on Fri Dec 15 15:22:05 GMT 2023 , Edited by admin on Fri Dec 15 15:22:05 GMT 2023
PRIMARY