858064
4(3H)-Pyrimidinone
≥98%
Sinonimo/i:
4(3H)-Pyrimidone, 4-Hydroxypyrimidine, 4-Pyrimidinol
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About This Item
Formula empirica (notazione di Hill):
C4H4N2O
Numero CAS:
Peso molecolare:
96.09
Beilstein:
609975
Numero CE:
Numero MDL:
Codice UNSPSC:
12352100
ID PubChem:
NACRES:
NA.22
Prodotti consigliati
Livello qualitativo
Saggio
≥98%
Stato
crystals
Punto di fusione
166-169 °C (lit.)
Temperatura di conservazione
2-8°C
Stringa SMILE
O=C1C=CNC=N1
InChI
1S/C4H4N2O/c7-4-1-2-5-3-6-4/h1-3H,(H,5,6,7)
DNCYBUMDUBHIJZ-UHFFFAOYSA-N
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Codice della classe di stoccaggio
11 - Combustible Solids
Classe di pericolosità dell'acqua (WGK)
WGK 3
Punto d’infiammabilità (°F)
Not applicable
Punto d’infiammabilità (°C)
Not applicable
Dispositivi di protezione individuale
Eyeshields, Gloves, type N95 (US)
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Aleem Gangjee et al.
Bioorganic & medicinal chemistry, 18(10), 3575-3587 (2010-04-21)
A series of eight N(4)-phenylsubstituted-6-(2,4-dichlorophenylmethyl)-7H-pyrrolo[2,3-d]pyrimidine-2,4-diamines 8-15 were synthesized as vascular endothelial growth factor receptor-2 (VEGFR-2) inhibitors with varied substitutions in the phenyl ring of the 4-anilino moiety. In addition, five N(4)-phenylsubstituted-6-phenylmethylsubstituted-7H-pyrrolo[2,3-d]pyrimidin-4-amines 16-20 were synthesized to evaluate the importance of the
C M Harris et al.
The Journal of biological chemistry, 272(36), 22514-22525 (1997-09-05)
Isolated from bovine milk, xanthine oxidase (XO) and xanthine dehydrogenase (XDH) are two interconvertible forms of the same protein, differing in the number of protein cysteines versus cystines. Most differences between XO and XDH are localized to the FAD center
Raquel Sanchez et al.
Journal of the American Chemical Society, 129(19), 6287-6290 (2007-04-24)
4-Hydroxypyrimidine (4HP) has two conformational forms (the hydroxyl hydrogen cis or trans with respect to the adjacent nitrogen), which are in tautomeric equilibrium with two ketonic forms, 4-pyrimidinone (4PO) and 6-pyrimidinone (6PO). We have investigated the free jet absorption millimeterwave
Barbara M Giuliano et al.
The journal of physical chemistry. A, 114(48), 12725-12730 (2010-11-10)
The keto-enol tautomerism of 4-hydroxypyrimidine and of the related molecules S-methyl-2-thiouracil and 2-thiouracil has been investigated using synchrotron-based techniques. The populations of the constituent tautomers and thermodynamic parameters have been obtained by analysis of core-level photoemission spectra. The effect of
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