 |
| Name | 4-Hydroxypyrimidine |
| Basic Information | |
| Synonyms | 4(1H)-PYRIMIDINONE; 4(3H)-PYRIMIDINONE; |
| CAS number | 51953-17-4 |
| EINECS | 257-545-4 |
| Formula | C4H4N2O |
| Molecular Weight | 96.09 |
| Melting Point | 166-169 °C(lit.) |
| Water Solubility | 270.3g/L(20 ºC) |
| Boiling Point | 179.58°C (rough estimate) |
| Density | 1.2604 (rough estimate) |
| Storage temp | 0-6°C |
| Refractive index | 1.4610 (estimate) |
| Safety Information | |
| Hazard Codes | Xi |
| Risk Statements | 36/37/38 |
| Safety Statements | 22-24/25-37/39-26-36 |
| RTECS | UW7350100 |
| HS Code | 29339900 |
| Description | |
| Pyrimidone is the name given to either of two heterocyclic compounds with the formula C4H4N2O: 2-pyrimidone and 4-pyrimidone. The compounds can also be called 2-hydroxypyrimidine or 4-hydroxypyrimidine respectively, based on a substituted pyrimidine, or 1, 3-diazine, ring. 4-pyrimidinone is an important bioactive molecule with various biological activities such as anti-virus, anti-tumor, induction of interferon production and immune regulation. | |
| Name | 4-Hydroxypyrimidine |
| Basic Information | |
| Synonyms | 4(1H)-PYRIMIDINONE; 4(3H)-PYRIMIDINONE; |
| CAS number | 51953-17-4 |
| EINECS | 257-545-4 |
| Formula | C4H4N2O |
| Molecular Weight | 96.09 |
| Melting Point | 166-169 °C(lit.) |
| Water Solubility | 270.3g/L(20 ºC) |
| Boiling Point | 179.58°C (rough estimate) |
| Density | 1.2604 (rough estimate) |
| Storage temp | 0-6°C |
| Refractive index | 1.4610 (estimate) |
| Safety Information | |
| Hazard Codes | Xi |
| Risk Statements | 36/37/38 |
| Safety Statements | 22-24/25-37/39-26-36 |
| RTECS | UW7350100 |
| HS Code | 29339900 |
| Description | |
| Pyrimidone is the name given to either of two heterocyclic compounds with the formula C4H4N2O: 2-pyrimidone and 4-pyrimidone. The compounds can also be called 2-hydroxypyrimidine or 4-hydroxypyrimidine respectively, based on a substituted pyrimidine, or 1, 3-diazine, ring. 4-pyrimidinone is an important bioactive molecule with various biological activities such as anti-virus, anti-tumor, induction of interferon production and immune regulation. | |
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