Weight | 111.104 g/mol |
---|---|
Formula | C4H5N3O |
Hydrogen Acceptors | 3 |
Hydrogen Donors | 2 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
Isocytosine (108-53-2)
Score:
#2074 in Physics
,
#6453 in Chemistry
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- The Infrared and Ultraviolet Absorption Spectra of Cytosine and Isocytosine in the Solid State1,2 (Journal of the American Chemical Society, 1952)
- Matrix isolation FT-IR studies and ab initio calculations of hydrogen-bonded complexes of molecules modeling cytosine or isocytosine tautomers. 1. Pyridine and pyrimidine complexes with water in argon matrixes (The Journal of Physical Chemistry, 1994)
- Theoretical and Experimental Study of Isoguanine and Isocytosine: Base Pairing in an Expanded Genetic System (Journal of the American Chemical Society, 1997)
- The crystal and molecular structure of isocytosine (Acta Crystallographica, 1965)
- Matrix-isolation FT-IR studies and ab-initio calculations of hydrogen-bonded complexes of molecules modeling cytosine or isocytosine tautomers. 2. 4-Aminopyridine and 4-aminopyrimidine complexes with H2O in Ar matrices (The Journal of Physical Chemistry, 1995)
- Nucleosides. 121. Improved and general synthesis of 2-deoxy C-nucleosides. Synthesis of 5-(2-deoxy--D-erythro-pentofuranosyl)uracil, -1-methyluracil, -1,3-dimethyluracil, and -isocytosine (Journal of Organic Chemistry, 1982)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CN=C(NC1=O)N
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InChIKeyXQCZBXHVTFVIFE-UHFFFAOYSA-N
- Pubchem - Isocytosine
- Wikipedia - 2-amino-4-hydroxypyrimidine
Isocytosine or 2-aminouracil is a pyrimidine base that is an isomer of cytosine. It is used in combination with isoguanine in studies of unnatural nucleic acid analogues of the normal base pairs in DNA. It can be synthesized from guanidine and malic acid.
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