6-Amino-5-hydroxy-2(1H)-pyrimidinone
Basic information
- CAS
13484-95-2- Standard SMILES
Nc1[nH]c(=O)ncc1O- InChIKey
NLLCDONDZDHLCI-UHFFFAOYSA-N- Molecular formula
- C4H5N3O2
- Average molar mass
- 127.1 g/mol
- Monoisotopic mass
- 127.03817641
Names & identifiers
- Preferred name
- 6-Amino-5-hydroxy-2(1H)-pyrimidinone
- IUPAC
- 6-amino-5-hydroxy-1H-pyrimidin-2-one
- English name
- 2(1H)-Pyrimidinone, 4-amino-5-hydroxy- (9CI)
- Molecular formula
- C4H5N3O2
- Molecular weight
- 127.1
Names & synonyms
5-Hydroxycytosine13484-95-2P72XNU89LE6-Amino-5-hydroxy-2(1H)-pyrimidinone2(1H)-Pyrimidinone, 4-amino-5-hydroxy-RefChem:9138212,5-Pyrimidinedione, 4-amino-1,6-dihydro-75321-30-16-amino-5-hydroxy-1H-pyrimidin-2-one4-Aminopyrimidine-2,5-diolCytosine, 5-hydroxy-5-hydroxy-cytosine
Show more names
2(1H)-Pyrimidinone, 6-amino-5-hydroxy-
2(1H)-Pyrimidinone, 6-amino-5-hydroxy-; 2(1H)-Pyrimidinone, 4-amino-5-hydroxy- (9CI); Cytosine, 5-hydroxy- (7CI,8CI); 6-Amino-5-hydroxy-2(1H)-pyrimidinone; 5-Hydroxycytosine4-Amino-5-hydroxy-2(1H)-pyrimidinoneUNII-P72XNU89LE2(1H)-Pyrimidinone, 4-amino-5-hydroxy- (9CI)SCHEMBL65897SCHEMBL3166078SCHEMBL8553831SCHEMBL20529713
Database identifiers
- CAS
13484-95-2- PubChem CID
- 3014752
- DTXSID
DTXSID00928775- UNII
- P72XNU89LE
- Nikkaji
- J702.446K
Properties
Computed structural properties
- XLogP
- -1.3
- Topological polar surface area
- 87.7 Ų
- Hydrogen bond donors
- 3
- Hydrogen bond acceptors
- 3
- Rotatable bonds
- 0
- Heavy atoms
- 9
- Formal charge
- 0
- Complexity
- 206
Physicochemical properties
- solubility
- DMSO (Slightly, Heated, Sonicated), Methanol (Slightly, Sonicated)
- form
- Solid
- color
- Light Yellow to Beige
- Stability
- Hygroscopic
- FDA UNII
- 72 XNU89LE · P72XNU89LE
Chemistry & industry
Applications
Uses5-Hydroxycytosine, is been identified as an anomalous base of phage H-17 DNA. It is also a monosubstituted cytosine, as nucleotide-base antimetabolite-type potential anticarcinogen.
Upstream & downstream products
Downstream products
Related reactions
0 records
No reaction records under the current filter.
Compound notes
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