223674-01-9

Usage

Uses

Used in Medical and Biochemical Research:
2,4,6-Pyrimidinetriol (9CI) is used as a research compound for understanding the structure and function of nucleic acids and their components. Its role in the study of pyrimidine nucleobases and their interactions with other biomolecules is crucial for advancing our knowledge in biochemistry and molecular biology.
Used in Laboratory Settings:
2,4,6-Pyrimidinetriol (9CI) is used as a reagent in various laboratory experiments, particularly in the synthesis of nucleic acid analogs and other related compounds. Its unique properties make it a valuable tool for researchers working on the development of new drugs and therapeutic agents.
Used in Pharmaceutical Development:
Although information on the potential toxicity or hazards of 2,4,6-Pyrimidinetriol (9CI) is limited, its potential use in pharmaceutical development cannot be overlooked. It may serve as a starting material or intermediate in the synthesis of novel compounds with potential therapeutic applications, particularly in the field of nucleic acid-based therapies.

InChI:InChI=1/C4H4N2O3/c7-2-1-3(8)6-4(9)5-2/h1H,(H3,5,6,7,8,9)

Downstream Products

• 29458-38-6 6-methoxypyrimidine-2,4-diol 
• 50270-27-4 2,4,6-trichloropyrimidine-5-carbaldehyde 

Relevant academic research and scientific papers

Silyl modification of biologically active compounds. 5. Hydrolytic stability and biological activity of the trialkylsilyl derivatives of some heterocyclic bases

The kinetics of the desilylation of the triorganosilyl derivatives of some biologically active heterocyclic bases and uridine were investigated by 1H NMR spectroscopy. A correlation was established between the relative rates of desilylation and the steric environment of the silicon atom. In trials on locomotor activity and muscular tone, the effect on memory processes, and the Porsolt test it was found that tris(tert-butylmethylsilyl)barbituric acid has higher sedative activity than barbituric acid. In contrast to uridine, 5′-O-tert-butyldimethylsilyluridine exhibits antitumor activity, suppressing the development of fibrosarcoma in human lungs (HT-1080) and fibroblasts in mice. 1999 Kluwer Academic/Plenum Publishers.

SUBSTANCES FOR DYEING KERATINOUS FIBERS

Disclosed are substances which contain unsaturated, non-aromatic dialdehydes of formula (Ia) and/or the tautomer (Ib) thereof, wherein R1, R2, and R3 are defined as indicated in claim 1, along with at least one CH-acidic compound of formulas (II) and/or (III), wherein R6, R7, R8, R9, R10, Y, X?, Het, and X1 are defined as indicated in claim 1, in a cosmetic carrier. Said substances color keratinous fibers, especially human hair, in an intensive, colorfast, natural brown shade.