CAS 496-76-4
:Isobarbituric acid
Description:
Isobarbituric acid, with the CAS number 496-76-4, is a chemical compound that belongs to the class of barbiturates, which are derivatives of barbituric acid. It is characterized by its structural formula, which features a pyrimidine ring with two carbonyl groups and an amino group. Isobarbituric acid is typically a white crystalline solid that is soluble in water and exhibits weak acidic properties. Its molecular structure allows it to participate in various chemical reactions, making it of interest in both pharmaceutical and biochemical research. The compound is known for its potential applications in the synthesis of other organic compounds and may also serve as an intermediate in the production of certain pharmaceuticals. Additionally, isobarbituric acid can exhibit biological activity, although its specific effects and mechanisms of action may vary. Safety data indicates that, like many chemical substances, it should be handled with care, following appropriate safety protocols to minimize exposure and risk.
Formula:C4H4N2O3
InChI:InChI=1S/C4H4N2O3/c7-2-1-5-4(9)6-3(2)8/h1H2,(H2,5,6,8,9)
InChI key:InChIKey=FQXOOGHQVPKHPG-UHFFFAOYSA-N
SMILES:O=C1C(=O)CNC(=O)N1
Synonyms:- 1,3-Diazinane-2,4,5-trione
- 2,4,5(3H)-Pyrimidinetrione, dihydro-
- 5-Hydroxyuracil
- 5-hydroxypyrimidine-2,4(1H,3H)-dione
- Dihydro-2,4,5(3H)-pyrimidinetrione
- Isobarbituric acid
- NSC 95958
- dihydropyrimidine-2,4,5(3H)-trione
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Found 11 products.
Isobarbituric Acid
CAS:Formula:C4H4N2O3Purity:>97.0%(GC)Color and Shape:White to Yellow to Orange powder to crystalMolecular weight:128.092,4,5-Trihydroxypyrimidine, 98%
CAS:<p>2,4,5-Trihydroxypyrimidine studies show that it can form stable base pairs with all four bases in a DNA duplex. It has been used as oxidative DNA damage biomarker in tissue engineered skin. It acts as an antagonist of uracil in the growth of Lactobacillus casei. This Thermo Scientific Chemicals bran</p>Formula:C4H4N2O3Purity:98%Color and Shape:Powder, White to pale creamMolecular weight:128.09FLUOROURACIL IMPURITY B CRS
CAS:<p>FLUOROURACIL IMPURITY B CRS</p>Formula:C4H4N2O3Molecular weight:128.0862Fluorouracil Related Compound B (Dihydropyrimidine-2,4,5(3H)-trione)
CAS:Compounds containing a pyrimidine ring (whether or not hydrogenated) or piperazine ring in the structure, nesoiFormula:C4H4N2O3Color and Shape:White PowderMolecular weight:128.02219Isobarbituric acid
CAS:<p>Isobarbituric acid is a glycosylase that cleaves the bond between the amino group and the hydroxyl group of uridine in DNA. It has been shown to react with nucleophilic groups at neutral pH, such as an amine or hydroxyl group. Isobarbituric acid can be used to measure oxidative damage to DNA. This compound is reactive and sensitive to UV light, which makes it useful for detecting damaged DNA. Isobarbituric acid has been shown to induce neuronal death in rodents by interfering with dendritic spine formation.</p>Formula:C4H4N2O3Purity:Min. 95%Color and Shape:White PowderMolecular weight:128.09 g/molIsobarbituric Acid
CAS:<p>Impurity Fluorouracil EP Impurity B; Fluorouracil USP Related Compound B<br>Applications A 5-hydroxy derivative of the nucleobase Uracil (U801000) and an isomer of Barbituric Acid (B118650). Studies show that it can form stable base pairs with all four bases in a DNA duplex. It has been used as oxidative DNA damage biomarker in tissue engineered skin. Fluorouracil EP Impurity B. Fluorouracil USP Related Compound B<br>References Varatharasa T. et al.: Chem. Comm., 3, 400 (2005); Jaruga, P. et al.: Nucleic Acid Res., 24, 1389 (1996); Rodriguez, H. et al.: Adv. Exp. Med. Biol., 534, 129 (2003);<br></p>Formula:C4H4N2O3Color and Shape:NeatMolecular weight:128.09
