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Details

Stereochemistry ACHIRAL
Molecular Formula C7H12O4
Molecular Weight 160.1678
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIETHYLMALONIC ACID

SMILES

CCC(CC)(C(O)=O)C(O)=O

InChI

InChIKey=LTMRRSWNXVJMBA-UHFFFAOYSA-N
InChI=1S/C7H12O4/c1-3-7(4-2,5(8)9)6(10)11/h3-4H2,1-2H3,(H,8,9)(H,10,11)

HIDE SMILES / InChI

Molecular Formula C7H12O4
Molecular Weight 160.1678
Charge 0
Count
Stereochemistry ACHIRAL
Additional Stereochemistry No
Defined Stereocenters 0 / 0
E/Z Centers 0
Optical Activity NONE

Approval Year

PubMed

PubMed

TitleDatePubMed
Spectroscopic, solvent influence and thermal studies of ternary copper(II) complexes of diester and dinitrogen base ligands.
2010-10-15
Synthesis and anti-HIV evaluation of new acyclic phosphonate nucleotide analogues and their bis(SATE) derivatives.
2010-08
(3aR*,7aS*)-1-(p-Tolyl-sulfon-yl)perhydro-indol-2-one.
2010-04-17
Diethyl 2-[(5-meth-oxy-2-methyl-1-phenyl-sulfonyl-1H-indol-3-yl)methyl-ene]malonate.
2009-05-29
tert-Butyl 3-[2,2-bis-(ethoxy-carbon-yl)-vinyl]-2-methyl-1H-indole-1-carboxyl-ate.
2009-03-25
Quantitative analysis of cation binding to the adenosine nucleotides using the variable ionic strength method: validation of the Debye-Hückel-Onsager theory of electrophoresis in the absence of counterion binding.
2007-04
Synthesis, characterization and thermolysis of 1,1-diamino-2,2-dinitroethylene (FOX-7) and its salts.
2006-09-21
Synthesis and evaluation of 2,6-piperidinedione derivatives as potentially novel compounds with analgesic and other CNS activities.
2006-03
Simple synthesis and anti-HIV activity of novel cyclopentene phosphonate nucleosides.
2006
Condensation reactions of monomeric hydroxo palladium complexes with active methyl and methylene compounds.
2004-11-07
Determination of acidity constants of enolisable compounds by capillary electrophoresis.
2004-10
Novel autoxidation and Michael addition of a butenolide-containing sugar leading to a C-branched-chain glucopyranosidulose, and X-ray structure of intermediates.
2003-08-12
Formal synthesis of angiogenesis inhibitor NM-3.
2003-07-25
Spectral, electrochemical and molecular orbital studies on solvatochromic mixed ligand copper(II) complexes of malonate and diamine derivatives.
2003-04
Probing the electrostatic shielding of DNA with capillary electrophoresis.
2003-03
Palladium-catalyzed arylation of malonates and cyanoesters using sterically hindered trialkyl- and ferrocenyldialkylphosphine ligands.
2002-01-25
A general and mild copper-catalyzed arylation of diethyl malonate.
2002-01-24
Effect of malonyl malonanilide dimers on the thermal stability of nitrocellulose.
2001-11-16
Synthesis and biological activities of novel structural analogues of 2-arachidonoylglycerol, an endogenous cannabinoid receptor ligand.
2001-08-06
X-H (X = C, N, O, P, S) bond activations induced by beta-heterosubstituted zirconaindenes.
2001-01-05
N-(3-Acyloxy-2-benzylpropyl)-N'-(4-hydroxy-3-methoxybenzyl) thiourea derivatives as potent vanilloid receptor agonists and analgesics.
2001-01
Patents
Substance Class Chemical
Created
by admin
on Mon Mar 31 21:21:42 GMT 2025
Edited
by admin
on Mon Mar 31 21:21:42 GMT 2025
Record UNII
QHT44LOC3W
Record Status Validated (UNII)
Record Version
  • Download
Name Type Language
NSC-1986
Preferred Name English
DIETHYLMALONIC ACID
MI  
Systematic Name English
DIETHYLMALONIC ACID [MI]
Common Name English
3,3-PENTANEDICARBOXYLIC ACID
Systematic Name English
2,2-DIETHYLPROPANEDIOIC ACID
Systematic Name English
PROPANEDIOIC ACID, DIETHYL-
Common Name English
Code System Code Type Description
PUBCHEM
68185
Created by admin on Mon Mar 31 21:21:42 GMT 2025 , Edited by admin on Mon Mar 31 21:21:42 GMT 2025
PRIMARY
MERCK INDEX
m4410
Created by admin on Mon Mar 31 21:21:42 GMT 2025 , Edited by admin on Mon Mar 31 21:21:42 GMT 2025
PRIMARY Merck Index
NSC
1986
Created by admin on Mon Mar 31 21:21:42 GMT 2025 , Edited by admin on Mon Mar 31 21:21:42 GMT 2025
PRIMARY
MESH
C030978
Created by admin on Mon Mar 31 21:21:42 GMT 2025 , Edited by admin on Mon Mar 31 21:21:42 GMT 2025
PRIMARY
EPA CompTox
DTXSID9060150
Created by admin on Mon Mar 31 21:21:42 GMT 2025 , Edited by admin on Mon Mar 31 21:21:42 GMT 2025
PRIMARY
FDA UNII
QHT44LOC3W
Created by admin on Mon Mar 31 21:21:42 GMT 2025 , Edited by admin on Mon Mar 31 21:21:42 GMT 2025
PRIMARY
CAS
510-20-3
Created by admin on Mon Mar 31 21:21:42 GMT 2025 , Edited by admin on Mon Mar 31 21:21:42 GMT 2025
PRIMARY
ECHA (EC/EINECS)
208-111-8
Created by admin on Mon Mar 31 21:21:42 GMT 2025 , Edited by admin on Mon Mar 31 21:21:42 GMT 2025
PRIMARY