CAS 50887-69-9
:4-Pyrimidinecarboxylic acid, 1,2,3,6-tetrahydro-2,6-dioxo-, hydrate (1:1)
Description:
4-Pyrimidinecarboxylic acid, 1,2,3,6-tetrahydro-2,6-dioxo-, hydrate (1:1), with CAS number 50887-69-9, is a heterocyclic organic compound characterized by its pyrimidine ring structure, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. This compound features a carboxylic acid functional group, contributing to its acidic properties. The presence of the tetrahydro structure indicates that it has undergone partial saturation, which can influence its reactivity and stability. The dioxo groups suggest the presence of two carbonyl functionalities, enhancing its potential for various chemical reactions, such as nucleophilic attacks. As a hydrate, it contains water molecules in its crystalline form, which can affect its solubility and physical properties. This compound may be of interest in pharmaceutical and agricultural chemistry due to its potential biological activity and applications in synthesis. Its specific characteristics, such as melting point, solubility, and reactivity, would depend on the conditions under which it is studied.
Formula:C5H4N2O4·H2O
InChI:InChI=1S/C5H4N2O4.H2O/c8-3-1-2(4(9)10)6-5(11)7-3;/h1H,(H,9,10)(H2,6,7,8,11);1H2
InChI key:InChIKey=YXUZGLGRBBHYFZ-UHFFFAOYSA-N
SMILES:C(O)(=O)C1=CC(=O)NC(=O)N1.O
Synonyms:- 2,6-Dioxo-1,2,3,6-Tetrahydropyrimidine-4-Carboxylate
- 2,6-Dioxo-1,2,3,6-Tetrahydropyrimidine-4-Carboxylic Acid Hydrate
- 2,6-Dioxo-1,2,3,6-tetrahydro-4-pyrimidinecarboxylic acid
- 2,6-Dioxo-1,2,3,6-tetrahydro-4-pyrimidinecarboxylic acid hydrate
- 2.4-Dihydroxypyrimidine-6-carboxylic acid hydrate
- 4-Pyrimidinecarboxylic acid, 1,2,3,6-tetrahydro-2,6-dioxo-, hydrate (1:1)
- 4-Pyrimidinecarboxylic acid, 1,2,3,6-tetrahydro-2,6-dioxo-, monohydrate
- Orotic Acid Monohydrate
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Found 11 products.
Orotic acid monohydrate
CAS:Formula:C5H6N2O5Purity:95%Color and Shape:Solid, White powderMolecular weight:174.112Orotic acid hydrate, 98%
CAS:<p>Orotic acid hydrate is used in cosmetic and food industry. It is also used as a pharmaceutical intermediate. This Thermo Scientific Chemicals brand product was originally part of the Alfa Aesar product portfolio. Some documentation and label information may refer to the legacy brand. The original Al</p>Formula:C5H4N2O4Purity:98%Color and Shape:White to pale cream, Crystals or powder or crystalline powderMolecular weight:156.102,6-Dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylic acid monohydrate
CAS:<p>2,6-Dioxo-1,2,3,6-tetrahydropyrimidine-4-carboxylic acid monohydrate</p>Formula:C5H4N2O4·H2OPurity:98%Color and Shape: white to off-white powderMolecular weight:174.11154g/molOrotic Acid Monohydrate
CAS:Formula:C5H4N2O4·H2OPurity:>98.0%(T)(HPLC)Color and Shape:White powder to crystalMolecular weight:174.12Orotic acid monohydrate
CAS:<p>Orotic acid monohydrate is an intermediate product in pyrimidine metabolism.</p>Formula:C5H6N2O5Purity:99.30%Color and Shape:White Crystalline PowderMolecular weight:174.11Orotic Acid Monohydrate
CAS:Controlled Product<p>Applications Orotic Acid is used in the preparation of therapeutic agents for chronic obstructive pulmonary disease (COPD) treatment.<br></p>Formula:C5H4N2O4·H2OColor and Shape:NeatMolecular weight:174.11Orotic Acid-13C5 Monohydrate
CAS:Controlled Product<p>Applications Orotic acid-13C5 monohydrate is a labelled analogue of Orotic acid monohydrate (O691500).<br></p>Formula:C5H3N2O4·H2OColor and Shape:NeatMolecular weight:178.067Orotic acid hydrate
CAS:<p>Orotic acid hydrate is a synthetic compound that is designed to be a growth regulator. Orotic acid hydrate is synthesized by reacting the orotate with pyridoxine hydrochloride, followed by crystallizing the product. Hydrogen bonds form between the water molecules and fatty acids in the crystals of OA hydrate. These hydrogen bonds stabilize the crystal structure and allow for its use as a growth regulator. The stability of this molecule can also be attributed to its ability to form hydrogen bonds with other molecules such as α-tocopherol, calcium carbonate, and synthetic cannabinoids. Orotic acid hydrate has been shown to have an effect on cancer cells because it reacts with daunorubicin in solution and inhibits DNA synthesis, inhibiting cell growth.</p>Formula:C5H4N2O4·H2OPurity:Min. 95 Area-%Color and Shape:PowderMolecular weight:174.11 g/mol








