| Identification | More | [Name]
5-FORMYLURACIL | [CAS]
1195-08-0 | [Synonyms]
1,2,3,4-TETRAHYDRO-2,4-DIOXOPYRIMIDINE-5-CARBALDEHYDE
5-FORMILURACIL
5-FORMYLURACIL
AURORA KA-650
RARECHEM AH CK 0106
5-Pyrimidinecarboxaldehyde, 1,2,3,4-tetrahydro-2,4-dioxo-(6CI,7CI,8CI,9CI)
5-Formyluracil 98%
2,4-Dioxo-1,2,3,4-tetrahydropyrimidine-5-carbaldehyde | [Molecular Formula]
C5H4N2O3 | [MDL Number]
MFCD00192185 | [Molecular Weight]
140.1 | [MOL File]
1195-08-0.mol |
| Chemical Properties | Back Directory | [Appearance]
White Powder | [Melting point ]
>300 °C (dec.) (lit.) | [density ]
1.567±0.06 g/cm3(Predicted) | [storage temp. ]
Inert atmosphere,Store in freezer, under -20°C | [solubility ]
DMSO (Slightly), Methanol (Slightly) | [form ]
Solid | [pka]
7.27±0.10(Predicted) | [color ]
White to Pale Yellow | [Sensitive ]
Air Sensitive | [Usage]
Nucleoside derivatives of 5-substituted uracil have been explored for their potential application as anti-viral agents and in the treatment of tumors | [InChIKey]
OHAMXGZMZZWRCA-UHFFFAOYSA-N | [CAS DataBase Reference]
1195-08-0(CAS DataBase Reference) |
| Safety Data | Back Directory | [Hazard Codes ]
Xi | [Risk Statements ]
R36/37/38:Irritating to eyes, respiratory system and skin . | [Safety Statements ]
S26:In case of contact with eyes, rinse immediately with plenty of water and seek medical advice .
S36:Wear suitable protective clothing . | [WGK Germany ]
3
| [Hazard Note ]
Irritant | [HS Code ]
29349990 |
| Hazard Information | Back Directory | [Chemical Properties]
White Powder | [Uses]
Nucleoside derivatives of 5-substituted uracil have been explored for their potential application as anti-viral agents and in the treatment of tumors | [Uses]
Nucleoside derivatives of 5-substituted uracil have been explored for their potential application as anti-viral agents and in the treatment of tumors. | [Definition]
ChEBI: A pyrimidone resulting from the formal oxidation of the alcoholic hydroxy group of 5-hydroxymethyluracil to the corresponding aldehyde. It is a major one-electron photooxidation product of thymine in oligodeoxynucleotides. | [Synthesis Reference(s)]
Tetrahedron Letters, 7, p. 5253, 1966 DOI: 10.1016/0005-2760(66)90119-6 |
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