CAS 56-09-7
:2-Amino-6-hydroxy-4(3H)-pyrimidinone
Description:
2-Amino-6-hydroxy-4(3H)-pyrimidinone, also known as allopurinol, is a heterocyclic organic compound characterized by its pyrimidine ring structure, which contains both amino and hydroxy functional groups. This compound is primarily recognized for its role as a xanthine oxidase inhibitor, making it significant in the treatment of gout and certain types of kidney stones by reducing uric acid production. It is typically a white to off-white crystalline powder, soluble in water and alcohol, and exhibits a melting point that varies depending on purity. The presence of the amino and hydroxy groups contributes to its reactivity and biological activity. In terms of safety, it is essential to handle this compound with care, as it can cause side effects in some individuals, including allergic reactions. Overall, 2-Amino-6-hydroxy-4(3H)-pyrimidinone is an important pharmaceutical agent with specific therapeutic applications, particularly in managing hyperuricemia.
Formula:C4H5N3O2
InChI:InChI=1S/C4H5N3O2/c5-4-6-2(8)1-3(9)7-4/h1H,(H4,5,6,7,8,9)
InChI key:InChIKey=AUFJTVGCSJNQIF-UHFFFAOYSA-N
SMILES:O=C1C=C(O)N=C(N)N1
Synonyms:- 2-Amino-4,6-dihydroxypyridimine
- 2-Amino-4,6-dioxypyrimidine
- 2-Amino-4,6-pyrimidinediol
- 2-Amino-4,6-pyrimidinedione
- 2-Amino-4-hydroxy-1H-pyrimidin-6-one
- 2-Amino-6-hydroxy-1,4-dihydropyrimidin-4-one
- 2-Amino-6-hydroxy-1H-pyrimidin-4-one
- 2-Amino-6-hydroxy-3H-pyrimidin-4-one
- 2-Amino-6-hydroxy-4(3H)-pyrimidinone
- 4(1H)-Pyrimidinone, 2-amino-6-hydroxy-
- 4(3H)-Pyrimidinone, 2-amino-6-hydroxy-
- 4,6-Dihydroxy-2-aminopyrimidine
- 4,6-Pyrimidinediol, 2-amino-
- NSC 15920
- NSC 18692
- See more synonyms
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Found 8 products.
2-Amino-4,6-dihydroxypyrimidine, 98%
CAS:<p>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 Alfa Aesar product / item code or SKU reference has not changed as a part of the brand transition to Thermo Sci</p>Formula:C4H5N3O2Purity:98%Color and Shape:White to cream or pale yellow to pale pink, PowderMolecular weight:127.102-Amino-4,6-dihydroxypyrimidine
CAS:Formula:C4H5N3O2Purity:95%Color and Shape:SolidMolecular weight:127.10142-Amino-4,6-dihydroxypyrimidine
CAS:Formula:C4H5N3O2Purity:>98.0%(HPLC)Color and Shape:White to Light yellow to Dark green powder to crystalMolecular weight:127.102-Amino-4,6-dihydroxypyrimidine
CAS:2-Amino-4,6-dihydroxypyrimidineFormula:C4H5N3O2Purity:98%Color and Shape: yellow solidMolecular weight:127.1014g/mol2-Amino-4,6-dihydroxypyrimidine
CAS:Formula:C4H5N3O2Purity:95%Color and Shape:SolidMolecular weight:127.1032-Amino-4,6-dihydroxypyrimidine-13C2
CAS:Controlled Product<p>Applications 2-Amino-4,6-dihydroxypyrimidine-13C2 is an intermediate in the production of antimicrobial guanylsulfonamides.<br>References Barrett, O., et al.: ChemBioChem., 7, 1882 (2006), Patel, P., et al.: Bioorg. Med. Chem. Lett., 17, 6610 (2007), Gasser, L., et al.: Environ. Sci. Technol., 41, 2445 (2007)<br></p>Formula:C2C2H5N3O2Color and Shape:NeatMolecular weight:129.0872-Amino-4,6-dihydroxypyrimidine
CAS:<p>2-Amino-4,6-dihydroxypyrimidine is a chemical compound that is used in the synthesis of pemetrexed. It has been shown to inhibit the growth of cancer cells in cell culture by cross-coupling with nitrogen atoms in DNA and thereby inhibiting replication. 2-Amino-4,6-dihydroxypyrimidine also reacts with halides to form reaction intermediates that are capable of reacting with hydrogen bonds and other functional groups. This chemical compound has been shown to have radical scavenging activities in acidic environments and vibrational properties.</p>Formula:C4H5N3O2Purity:Min. 98 Area-%Color and Shape:PowderMolecular weight:127.1 g/mol







