CAS 52944-66-8
:2,4,6(1H,3H,5H)-Pyrimidinetrione,5-(ethyl-d5)-5-(1-methylbutyl)- (9CI)
Description:
2,4,6(1H,3H,5H)-Pyrimidinetrione, 5-(ethyl-d5)-5-(1-methylbutyl)-, also known by its CAS number 52944-66-8, is a synthetic organic compound that belongs to the class of pyrimidinetriones. This compound features a pyrimidine ring, which is a six-membered aromatic heterocycle containing two nitrogen atoms at positions 1 and 3. The presence of the trione functional groups indicates that it has three carbonyl (C=O) groups, contributing to its reactivity and potential applications in various chemical reactions. The ethyl-d5 and 1-methylbutyl substituents suggest that this compound has been isotopically labeled, which can be useful in tracing studies or metabolic research. The compound's structure may impart specific physical and chemical properties, such as solubility in organic solvents and potential interactions with biological systems. Its applications could range from pharmaceuticals to agrochemicals, depending on its biological activity and stability. However, detailed studies would be necessary to fully understand its characteristics and potential uses.
Formula:C11H13D5N2O3
Synonyms:- Pentobarbital-D5
- Pentobarbital-D5 (Ethyl-D5)
- Phenobarbital (D5)
- Phenobarbital-D5 (Ethyl-D5)
- Phenobarbital (Ethyl-D5)
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Found 6 products.
Pentobarbital-d5
CAS:Controlled ProductApplications Pentobarbital-d5 is labelled Pentobarbital (P276000, sodium salt) which is a short-acting barbiturate. Typical applications for pentobarbital are sedative, hypnotic for short term, preanesthetic and control of convulsions in emergencies.
References Schafer, E.W., et al.: Toxicol. Appl. Pharmacol., 21, 315 (1972), Woster, P.S., et al.: Clin. Pharm., 9, 762 (1990), Evans, A.T., et al.: J. Am. Vet. Med. Assoc., 203, 664 (1993),Formula:C112H5H13N2O3Color and Shape:WhiteMolecular weight:231.3

