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Potassium 2,6-Dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylate

Potassium 2,6-Dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylate - CAS 24598-73-0

Catalog:	BB018544
Product Name:	Potassium 2,6-Dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylate
CAS:	24598-73-0
Synonyms:	potassium;2,4-dioxo-1H-pyrimidine-6-carboxylate; potassium;2,4-dioxo-1H-pyrimidine-6-carboxylate

Technical Data

Patents

Literatures

Computed Properties

IUPAC Name:	potassium;2,4-dioxo-1H-pyrimidine-6-carboxylate
Description:	Potassium 2,6-Dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylate (CAS# 24598-73-0) is a useful research chemical.
Molecular Weight:	194.19
Molecular Formula:	C5H3N2O4K
Canonical SMILES:	C1=C(NC(=O)NC1=O)C(=O)[O-].[K+]
InChI:	InChI=1S/C5H4N2O4.K/c8-3-1-2(4(9)10)6-5(11)7-3;/h1H,(H,9,10)(H2,6,7,8,11);/q;+1/p-1
InChI Key:	DHBUISJCVRMTAZ-UHFFFAOYSA-M
Density:	2.3534 g/cm³
MDL:	MFCD00039118
LogP:	-2.57330

Publication Number	Title	Priority Date
WO-2021194375-A1	Drug for treating coronaviral and retroviral infections and hepatitis c	20200326
RU-2731065-C1	Cryopreservant composition for long-term storage of primary keratinocytes	20191224
BE-1027127-A1	Propulsion system for electrically assisted vehicle	20190816
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RU-2712210-C1	Medicament for acceptance stimulating of the mesh implant after plastic repair of the ventral hernias	20190710

PMID	Publication Date	Title	Journal
25601987	20150401	Orotic acid induces hypertension associated with impaired endothelial nitric oxide synthesis	Toxicological sciences : an official journal of the Society of Toxicology
25786523	20150401	Dehydroepiandrosterone sulfate and cytochrome P450 inducers alleviate fatty liver in male rats fed an orotic acid-supplemented diet	The Journal of toxicological sciences
22922643	20121101	Solid state simulation of tetramer form of 5-aminoorotic acid: the vibrational spectra and molecular structure study by using MP2 and DFT calculations	Spectrochimica acta. Part A, Molecular and biomolecular spectroscopy
22692683	20120915	Miller (Genee-Wiedemann) syndrome represents a clinically and biochemically distinct subgroup of postaxial acrofacial dysostosis associated with partial deficiency of DHODH	Human molecular genetics
22634191	20120901	Ion-exclusion chromatography determination of organic acid in uridine 5'-monophosphate fermentation broth	Journal of chromatographic science

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Related Functional Groups

Carbonyl Compounds

[91125-43-8]
Sulfophenyl nonanoate sodium salt
[1018141-88-2]
1-(2-Cyanoethyl)-3-methyl-6-phenyl-1H-pyrazolo[3,4-b]pyridine-4-carboxylic acid
[1006443-01-1]
1-(5-Nitropyridin-2-yl)-1H-pyrazole-3-carboxylic acid
[832741-29-4]
1-(4-Bromo-5-propylthiophen-2-yl)ethanone
[1431966-64-1]
1-{2-[(3-Methoxypropyl)amino]-4-methyl-1,3-thiazol-5-yl}ethanone hydrochloride
[927676-51-5]
2-(6-Bromo-3-indolyl)-2-oxoacetic Acid

Complexity:	273
Compound Is Canonicalized:	Yes
Covalently-Bonded Unit Count:	2
Defined Atom Stereocenter Count:	0
Defined Bond Stereocenter Count:	0
Exact Mass:	193.97298807
Formal Charge:	0
Heavy Atom Count:	12
Hydrogen Bond Acceptor Count:	4
Hydrogen Bond Donor Count:	2
Isotope Atom Count:	0
Monoisotopic Mass:	193.97298807
Rotatable Bond Count:	1
Topological Polar Surface Area:	98.3
Undefined Atom Stereocenter Count:	0
Undefined Bond Stereocenter Count:	0