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Details

Stereochemistry ACHIRAL
Molecular Formula C3H4O6
Molecular Weight 136.0603
Optical Activity NONE
Defined Stereocenters 0 / 0
E/Z Centers 0
Charge 0

SHOW SMILES / InChI
Structure of DIHYDROXYMALONIC ACID

SMILES

OC(=O)C(O)(O)C(O)=O

InChI

InChIKey=VUCKYGJSXHHQOJ-UHFFFAOYSA-N
InChI=1S/C3H4O6/c4-1(5)3(8,9)2(6)7/h8-9H,(H,4,5)(H,6,7)

HIDE SMILES / InChI

Approval Year

PubMed

PubMed

TitleDatePubMed
[Cu3(Hmesox)3]3-: a precursor for the rational design of chiral molecule-based magnets (H4mesox = 2-dihydroxymalonic acid).
2010-09-06
Tetrahydroxy-p-benzoquinone as a source of polydentate O-donor ligands. Synthesis, crystal structure, and magnetic properties of the [Cu(bpy)(dhmal)]2 dimer and the two-dimensional [{SiW12O40}{Cu2(bpy)2(H2O)(ox)}2].16H2O inorganic-metalorganic hybrid.
2007-02-19
Pyrophosphate analogues as inhibitors of herpes simplex virus type 1 DNA polymerase.
1980-03-28
Patents

Patents

Name Type Language
MESOXALIC ACID HYDRATE [MI]
Preferred Name English
DIHYDROXYMALONIC ACID
Systematic Name English
PROPANEDIOIC ACID, DIHYDROXY-
Common Name English
PROPANEDIOIC ACID, 2,2-DIHYDROXY-
Common Name English
PROPANEDIOIC ACID, OXO-, HYDRATE
Common Name English
MESOXALIC ACID, HYDRATE
Common Name English
2,2-DIHYDROXYPROPANEDIOIC ACID
Systematic Name English
Code System Code Type Description
WIKIPEDIA
DIHYDROXYMALONIC ACID
Created by admin on Mon Mar 31 21:19:21 GMT 2025 , Edited by admin on Mon Mar 31 21:19:21 GMT 2025
PRIMARY
PUBCHEM
68412
Created by admin on Mon Mar 31 21:19:21 GMT 2025 , Edited by admin on Mon Mar 31 21:19:21 GMT 2025
PRIMARY
ECHA (EC/EINECS)
209-208-8
Created by admin on Mon Mar 31 21:19:21 GMT 2025 , Edited by admin on Mon Mar 31 21:19:21 GMT 2025
PRIMARY
EPA CompTox
DTXSID70905078
Created by admin on Mon Mar 31 21:19:21 GMT 2025 , Edited by admin on Mon Mar 31 21:19:21 GMT 2025
PRIMARY
MERCK INDEX
m7253
Created by admin on Mon Mar 31 21:19:21 GMT 2025 , Edited by admin on Mon Mar 31 21:19:21 GMT 2025
PRIMARY Merck Index
FDA UNII
OT429C180H
Created by admin on Mon Mar 31 21:19:21 GMT 2025 , Edited by admin on Mon Mar 31 21:19:21 GMT 2025
PRIMARY
CAS
560-27-0
Created by admin on Mon Mar 31 21:19:21 GMT 2025 , Edited by admin on Mon Mar 31 21:19:21 GMT 2025
PRIMARY