MESOXALIC ACID

Details

Stereochemistry	ACHIRAL
Molecular Formula	C3H2O5
Molecular Weight	118.045
Optical Activity	NONE
Defined Stereocenters	0 / 0
E/Z Centers	0
Charge	0

SHOW SMILES / InChI

Structure Search

SMILES

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

InChI

InChIKey=XEEVLJKYYUVTRC-UHFFFAOYSA-N

InChI=1S/C3H2O5/c4-1(2(5)6)3(7)8/h(H,5,6)(H,7,8)

HIDE SMILES / InChI

Molecular Formula	C3H2O5
Molecular Weight	118.045
Charge	0
Count

Stereochemistry	ACHIRAL
Additional Stereochemistry	No
Defined Stereocenters	0 / 0
E/Z Centers	0
Optical Activity	NONE

Approval Year

PubMed

Title	Date	PubMed
Structure-function relations in oxaloacetate decarboxylase complex. Fluorescence and infrared approaches to monitor oxomalonate and Na(+) binding effect.	2010-06-03	20543879
Reactions of iodomalonic acid, diiodomalonic acid, and other organics in the Briggs-Rauscher oscillating system.	2010-02-25	20121222
Effects of precursor concentration and acidic sulfate in aqueous glyoxal-OH radical oxidation and implications for secondary organic aerosol.	2009-11-01	19924930
Oxidation of glycerol by 2,2,6,6-tetramethylpiperidine-N-oxyl (TEMPO) in the presence of laccase.	2009-10	19464170
Hydroxyapatite nanoparticles as particulate emulsifier: fabrication of hydroxyapatite-coated biodegradable microspheres.	2009-09-01	19514753
Phragmites australis root secreted phytotoxin undergoes photo-degradation to execute severe phytotoxicity.	2009-06	19816146
Kinetics and mechanism of degradation of p-chloronitrobenzene in water by ozonation.	2008-04-15	17889996
Degradation of macromolecular tannic acid by O3/H2O2.	2008	18587196
On the basics of carbohydrate-metal chemistry: complexes of palladium(II) with hydroxyaldehyde and -ketone hydrates.	2007-08-13	17532305
Determinants of substrate specificity for saccharopine dehydrogenase from Saccharomyces cerevisiae.	2007-06-26	17542618
Uncatalyzed reactions in the classical Belousov-Zhabotinsky system. 2. The malonic acid-bromate reaction in acidic media.	2006-01-26	16419999
Reaction of serine-glyoxylate aminotransferase with the alternative substrate ketomalonate indicates rate-limiting protonation of a quinonoid intermediate.	2005-12-06	16313196
Oxaloacetate decarboxylase of Vibrio cholerae: purification, characterization, and expression of the genes in Escherichia coli.	2005-02	15647905
Amination and [2,3]-sigmatropic rearrangement of propargylic sulfides using a ketomalonate-derived oxaziridine: synthesis of N-allenylsulfenimides.	2003-09-21	14527143
Efficient amination of sulfides with a ketomalonate-derived oxaziridine: application to [2,3]-sigmatropic rearrangements of allylic sulfimides.	2002-04-21	12123037

Patents

Substance Class	Chemical Created by `admin` on `Mon Mar 31 19:35:18 GMT 2025` Edited by `admin` on `Mon Mar 31 19:35:18 GMT 2025`
Record UNII	62R514HE48
Record Status	`Validated (UNII)`
Record Version

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Name

Type

Language

MESOXALIC ACID [MI]

Preferred Name

English

MESOXALIC ACID

Systematic Name

English

2-OXOPROPANEDIOIC ACID

Systematic Name

English

KETOMALONIC ACID

Systematic Name

English

OXOMALONIC ACID

Systematic Name

English

Code System Code Type Description

CAS

473-90-5