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{{chembox |
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{{chembox |
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| Verifiedfields = changed |
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| verifiedrevid = 384093002 |
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| Watchedfields = changed |
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|ImageFile=Dihydrouracil.svg |
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| verifiedrevid = 416414074 |
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|ImageSize=120px |
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| ImageFile=Dihydrouracil.svg |
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|IUPACName=hexahydropyrimidine-2,4-dione |
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| ImageSize=120px |
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|OtherNames= |
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| PIN = 1,3-Diazinane-2,4-dione |
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| OtherNames= Dihydropyrimidine-2,4(1''H'',3''H'')-dione |
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|Section1={{Chembox Identifiers |
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|Section1={{Chembox Identifiers |
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| CASNo_Ref = {{cascite|correct|??}} |
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| CASNo=504-07-4 |
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| CASNo=504-07-4 |
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| PubChem=649 |
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| UNII_Ref = {{fdacite|correct|FDA}} |
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| SMILES=C1CNC(=O)NC1=O |
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| UNII = 016FR52RU5 |
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| MeSHName=Dihydrouracil |
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| PubChem=649 |
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| SMILES=C1CNC(=O)NC1=O |
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| ChemSpiderID_Ref = {{chemspidercite|changed|chemspider}} |
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| ChemSpiderID = 629 |
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| InChI = 1/C4H6N2O2/c7-3-1-2-5-4(8)6-3/h1-2H2,(H2,5,6,7,8) |
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| InChIKey = OIVLITBTBDPEFK-UHFFFAOYAM |
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| StdInChI_Ref = {{stdinchicite|changed|chemspider}} |
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| StdInChI = 1S/C4H6N2O2/c7-3-1-2-5-4(8)6-3/h1-2H2,(H2,5,6,7,8) |
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| StdInChIKey_Ref = {{stdinchicite|changed|chemspider}} |
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| StdInChIKey = OIVLITBTBDPEFK-UHFFFAOYSA-N |
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| MeSHName=Dihydrouracil |
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|Section2={{Chembox Properties |
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|Section2={{Chembox Properties |
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| Formula=C<sub>4</sub>H<sub>6</sub>N<sub>2</sub>O<sub>2</sub> |
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| Formula=C<sub>4</sub>H<sub>6</sub>N<sub>2</sub>O<sub>2</sub> |
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| MolarMass=114.10264 |
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| MolarMass=114.10264 |
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|Section3={{Chembox Hazards |
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|Section3={{Chembox Hazards |
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| AutoignitionPt = |
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'''Dihydrouracil''' is an intermediate in the catabolism of ].<ref>{{cite journal |last1=Nakamura |first1=A |last2=Kikuchi |first2=K |last3=Ohishi |first3=T |last4=Masuike |first4=T |title=. |journal=Gan to Kagaku Ryoho. Cancer & Chemotherapy |date=March 2004 |volume=31 |issue=3 |pages=381–6 |pmid=15045945}}</ref> It is the base present in the ] ]. |
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'''Dihydrouracil''' is an intermediate in the catabolism of ]. |
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==See also== |
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==See also== |
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* ] |
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==References== |
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{{reflist}} |
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{{Nucleotide metabolism intermediates}} |
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{{Nucleotide metabolism intermediates}}{{Nucleobases, nucleosides, and nucleotides}} |
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] |
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{{organic-compound-stub}} |
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{{organic-compound-stub}} |
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] |
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