Pyrimidone
{{chembox
| Watchedfields = changed
| verifiedrevid = 418471733
| Name = 4-Pyrimidone
| ImageFile = 4-Pyrimidone.png
| ImageSize = 120px
| PIN = 1H-Pyrimidin-6-one
| OtherNames = Hydroxypyrimidine; Pyrimidinone
|Section1={{Chembox Identifiers
| CASNo_Ref = {{cascite|correct|CAS}}
| CASNo = 557-01-7
| CASNo_Comment = 2-Pyrimidone
| CASNo1_Ref = {{fdacite|correct|CAS}}
| CASNo1 = 4562-27-0
| CASNo1_Comment = 4-Pyrimidone
| UNII_Ref = {{fdacite|correct|FDA}}
| UNII = 13K708ILY4
| UNII_Comment = 2-Pyrimidone
| UNII1_Ref = {{fdacite|correct|FDA}}
| UNII1 = K43V90OY4L
| UNII1_Comment = 4-Pyrimidone
| PubChem = 20695
| SMILES = O=C1NC=NC=C1
| ChemSpiderID = 61686
| ChemSpiderID_Comment = 2-Pyrimidone
| ChemSpiderID1 = 19489
| ChemSpiderID1_Comment = 4-Pyrimidone
}}
|Section2={{Chembox Properties
| C=4 | H=4 | N=2 | O=1
| Appearance = White to light yellow powder
| Density =
| MeltingPtC = 163 to 168
| MeltingPt_notes =
| BoilingPt =
| Solubility = }}
|Section3={{Chembox Hazards
| MainHazards = Respiratory system, eye, skin irritation
| FlashPt =
| AutoignitionPt =
}}
}}
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.
Derivatives
Derivatives of pyrimidone are the basis of many other biological molecules, including:
- Nucleobases, such as cytosine
- Barbiturates, such as metharbital
File:Cytosine chemical structure.png|Cytosine
File:Metharbital.svg|Metharbital
- Antiulcer drugs including temelastine, icotidine, donetidine, and lupitidine.
{{Heterocyclic-stub}}