Weight | 205.986 g/mol |
---|---|
Formula | C4H3IN2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
5-iodopyrimidine (31462-58-5)
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- Roles of II and AgI interactions on the self-assembly of Ag(I) complexes containing 2-amino-5-iodopyrimidine; formation of the unique AgIIAg interaction (CrystEngComm, 2006)
- 06,5-Cyclonucleosides. Reactions of 5-iodopyrimidine nucleosides with base (Tetrahedron Letters, 1968)
- Synthesis of [14C]-, [13C4]-, and [13C4, 15N2]- 5-amino-4-iodopyrimidine (Journal of Labelled Compounds and Radiopharmaceuticals, 2008)
- 5-Bromo-2-iodopyrimidine: a novel, useful intermediate in selective palladium-catalysed cross-coupling reactions for efficient convergent syntheses (Chemical Communications, 1996)
- Heterocyclic polyfluoro-compounds. Part XXVIII [1]. Nucleophilic substitution in 2,5-difluoro-4,6-di-iodopyrimidine (Journal of Fluorine Chemistry, 1978)
- New type of interaction of 5-iodopyrimidine nucleosides with alkynes (Russian Chemical Bulletin, 1993)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=C(C=NC=N1)I
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InChIKeyDNWRLMRKDSGSPL-UHFFFAOYSA-N
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Similar Compounds
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cytosine
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