Compounds > tris(oxalato)chromate(iii)
Page last updated: 2024-11-06

tris(oxalato)chromate(iii)

Description Research Excerpts Clinical Trials Roles Classes Pathways Study Profile Bioassays Related Drugs Related Conditions Protein Interactions Research Growth Market Indicators

Description

Tris(oxalato)chromate(III), also known as potassium tris(oxalato)chromate(III) trihydrate, is a coordination compound with the formula K3[Cr(C2O4)3]ยท3H2O. It is a green, crystalline solid that is soluble in water. The compound is synthesized by reacting potassium chromate(VI) with oxalic acid in acidic solution. It is a popular compound studied in coordination chemistry due to its interesting optical properties and its use as a catalyst in various reactions. It exhibits a variety of applications, including use as a catalyst in organic reactions, and as a reagent in analytical chemistry. The complex is known for its distinctive photochemical behavior, making it an object of study in photochemistry and for its ability to catalyze the decomposition of hydrogen peroxide.'

tris(oxalato)chromate(III): RN given refers to tri-K salt [Medical Subject Headings (MeSH), National Library of Medicine, extracted Dec-2023]

Cross-References

ID SourceID
PubMed CID84267
MeSH IDM0153869

Synonyms (18)

Synonym
nsc-43606
14217-01-7
chromic potassium oxalate
tris(oxalato)chromate(iii)
4pgj85vv72 ,
unii-4pgj85vv72
nsc 43606
chromate(3-), tris(ethanedioato(2-)-o,o')-, tripotassium, (oc-6-11)-
potassium tris(oxalato)chromate(iii)
chromate(3-), tris(oxalato)-, tripotassium
chromic potassium oxalate [mi]
potassium oxalatochromate(iii) (k3(cr(c2o4)3))
potassium chromic oxalate
tripotassium tris(oxalato)chromate(iii)
potassium trioxalatochromate(iii)
tripotassium tris(ethanedioato)chromate(3-)
potassium (oc-6-11)-tris(ethanedioato(2-)-.kappa.o1,.kappa.o2)chromate(3-) (3:1)
Q27260333

Research Excerpts

Dosage Studied

ExcerptRelevanceReference
" The length of comet tail of DNA strand-broken cells increased in a dose-response relation with the increase of K2Cr2O7, whereas, the apoptotic index increased with the dosage of dexamethasone."( [Distinguishing apoptotic cells from DNA strand-broken cells by comet assay].
Heng, Z; Li, R; Zhang, Z, 2001)		0.31
[information is derived through text-mining from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Research

Studies (6)

TimeframeStudies, This Drug (%)All Drugs %
pre-19902 (33.33)18.7374
1990's1 (16.67)18.2507
2000's3 (50.00)29.6817
2010's0 (0.00)24.3611
2020's0 (0.00)2.80
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]

Market Indicators

Research Demand Index: 50.95

According to the monthly volume, diversity, and competition of internet searches for this compound, as well the volume and growth of publications, there is estimated to be very strong demand-to-supply ratio for research on this compound.

MetricThis Compound (vs All)
Research Demand Index50.95 (24.57)
Research Supply Index1.95 (2.92)
Research Growth Index4.32 (4.65)
Search Engine Demand Index74.40 (26.88)
Search Engine Supply Index1.97 (0.95)

This Compound (50.95)

All Compounds (24.57)

Study Types

Publication TypeThis drug (%)All Drugs (%)
Trials0 (0.00%)5.53%
Reviews0 (0.00%)6.00%
Case Studies0 (0.00%)4.05%
Observational0 (0.00%)0.25%
Other6 (100.00%)84.16%
[information is prepared from research data collected from National Library of Medicine (NLM), extracted Dec-2023]
SubstanceRelationship StrengthStudiesTrialsClassesRoles
5,5-dimethyl-1-pyrroline-1-oxide
5,5-dimethyl-1-pyrroline-1-oxide: do not confuse with DMPO (4',5'-dihydroxy-7-methoxy-4-phenyl-5,2'-oxidocoumarin). 5,5-dimethyl-1-pyrroline N-oxide : A member of the class of 1-pyrroline nitrones (1-pyrroline N-oxides) resulting from the formal N-oxidation of 5,5-dimethyl-1-pyrroline. Used as a spin trap for the study of radicals formed by enzymatic acetaldehyde oxidation.		1.97101-pyrroline nitronesneuroprotective agent;
spin trapping reagent
chromates
Chromates: Salts of chromic acid containing the CrO(2-)4 radical.. chromate(2-) : A chromium oxoanion resulting from the removal of two protons from chromic acid.		3.2460chromium oxoanion;
divalent inorganic anion		oxidising agent
dimyristoylmethylphosphatidic acid
dimyristoylmethylphosphatidic acid: RN given refers to parent cpd without isomeric designation		1.9910
hydroxyl radical
Hydroxyl Radical: The univalent radical OH. Hydroxyl radical is a potent oxidizing agent.		1.9710oxygen hydride;
oxygen radical;
reactive oxygen species
triacetoneamine-n-oxyl
Triacetoneamine-N-Oxyl: Cyclic N-oxide radical functioning as a spin label and radiation-sensitizing agent.. 4-oxo-TEMPO : A member of the class of aminoxyls that is TEMPO carrying an oxo group at position 4.		1.9710aminoxyls;
piperidones		radical scavenger
oxalates
Oxalates: Derivatives of OXALIC ACID. Included under this heading are a broad variety of acid forms, salts, esters, and amides that are derived from the ethanedioic acid structure.		3.2460
ConditionIndicatedRelationship StrengthStudiesTrials
Breast Cancer
[description not available]		01.9710
Breast Neoplasms
Tumors or cancer of the human BREAST.		01.9710