3D-FA61065 - 5-acetyl-13-dimethylbarbituric-acid
5-Acetyl-1,3-dimethylbarbituric Acid
CAS:Fórmula:C8H10N2O4Pureza:>98.0%(GC)(T)Cor e Forma:White to Light yellow powder to crystallinePeso molecular:198.181,3-Dimethylbarbituric Acid
CAS:Fórmula:C6H8N2O3Pureza:>98.0%(GC)(T)Cor e Forma:White to Light yellow to Light orange powder to crystalPeso molecular:156.141,3-Dimethylbarbituric acid, 99% (dry wt.), water <6%
CAS:1,3-Dimethylbarbituric acid is used as a catalyst in the Knoevenagel condensation of a series of aromatic aldehydes. It is also used in the synthesis of 5-aryl-6-(alkyl- or aryl-amino)-1,3-dimethylfuro [2,3-d]pyrimidine derivatives and enantioselective synthesis of isochromene pyrimidinedione deriva
Fórmula:C6H8N2O3Pureza:99%Cor e Forma:White to cream or pale yellow, Crystals or powder or crystalline powderPeso molecular:156.14Urapidil Impurity 4 (1,3-Dimethylbarbituric Acid)
CAS:Fórmula:C6H8N2O3Cor e Forma:White To Off-White SolidPeso molecular:156.141,3-Dimethylbarbituric acid
CAS:Fórmula:C6H8N2O3Pureza:≥ 99.0%Cor e Forma:White to off-white crystalline powderPeso molecular:156.141,3-Dimethyl Barbituric Acid
CAS:Produto ControladoApplications 1,3-Dimethyl Barbituric Acid (Urapidil Impurity 4) is a derivative of Barbituric acid (B118650). All of the barbituric acid derivatives which have been reported to have pronounced hypnotic activity are disubstituted in the 5-position.
References Gupta, K., et al.: Eur. J. Med. Chem., 17, 448 (1982), Weber, L., et al.: Curr. Med. Chem., 9, 2085 (2002), Skiles, J., et al.: Curr. Med. Chem., 11, 2911 (2004),Fórmula:C6H8N2O3Cor e Forma:NeatPeso molecular:156.141,3-Dimethyl-2,4,6(1H,3H,5H)-pyrimidinetrione
CAS:Produto Controlado1,3-Dimethyl-2,4,6(1H,3H,5H)-pyrimidinetrione is a heterocyclic organic compound, which is synthesized via established chemical procedures involving catalytic methods or direct condensation reactions. This compound is well-known for its role in the biochemical field as a urease inhibitor. Urease, an enzyme that catalyzes the hydrolysis of urea, is targeted by this compound to potentially mitigate issues related to excessive ammonia production in agricultural and medical settings.In addition to its enzymatic inhibition properties, 1,3-Dimethyl-2,4,6(1H,3H,5H)-pyrimidinetrione serves as a pivotal intermediate in barbiturate synthesis. Barbiturates are psychoactive compounds used historically in medicine for their sedative and anesthetic properties. The compound's structure allows it to participate in the Knoevenagel condensation, facilitating the formation of complex molecules essential in pharmaceutical development. These multifunctional applications make it a valuable tool in various scientific research contexts, exploring both inhibitory mechanisms and synthetic pathways for drug discovery and development.Fórmula:C6H8N2O3Pureza:Min. 98 Area-%Cor e Forma:PowderPeso molecular:156.14 g/mol5-acetyl-6-hydroxy-1,3-dimethyl-1,2,3,4-tetrahydropyrimidine-2,4-dione
CAS:Produto ControladoApplications 5-acetyl-6-hydroxy-1,3-dimethyl-1,2,3,4-tetrahydropyrimidine-2,4-dione (cas# 58713-03-4) is a useful research chemical.
Fórmula:C8H10N2O4Cor e Forma:NeatPeso molecular:198.18Hexobarbital-D3
CAS:Produto ControladoApplications Hexobarbital-D3 is a labelled analogue of Hexobarbital (H295350), a barbiturate derivative that exhibits hypnotic and anasthetic effects.
References Laroche, M. & Brodie, B.: J. Pharm. Exp. Ther., 130, 134 (1960); Pira, R. & Lieber, L.: J. Nutr., 105, 1544 (1975)Fórmula:C12D3H13N2O3Cor e Forma:NeatPeso molecular:239.286
