CAS 101803-06-9
:Pyrimidine, 5-iodo-2-methoxy-
Description:
Pyrimidine, 5-iodo-2-methoxy- is a heterocyclic organic compound characterized by a pyrimidine ring, which is a six-membered aromatic ring containing two nitrogen atoms at positions 1 and 3. The presence of an iodine atom at the 5-position and a methoxy group (-OCH3) at the 2-position contributes to its unique chemical properties. This compound is typically used in organic synthesis and may serve as an intermediate in the production of pharmaceuticals or agrochemicals. Its structure allows for various chemical reactions, including nucleophilic substitutions and electrophilic aromatic substitutions, due to the electron-withdrawing nature of the iodine atom and the electron-donating properties of the methoxy group. The compound's solubility and reactivity can be influenced by these substituents, making it a valuable building block in synthetic chemistry. Additionally, its potential biological activity may be explored in medicinal chemistry, although specific biological properties would require further investigation.
Formula:C5H5IN2O
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Found 4 products.
Pyrimidine, 5-iodo-2-methoxy-
CAS:Formula:C5H5IN2OPurity:98%Color and Shape:SolidMolecular weight:236.01055-Iodo-2-methoxypyrimidine
CAS:<p>5-Iodo-2-methoxypyrimidine</p>Formula:C5H5IN2OPurity:95%Color and Shape: light yellow to light brown powderMolecular weight:236.01g/mol5-Iodo-2-methoxypyrimidine
CAS:<p>5-Iodo-2-methoxypyrimidine is an enantioenriched, modular, polyfunctionalized, derivatized molecule that has been shown to be both antiproliferative and selective. It is synthesized in a two step reaction from acetate and 2-iodo-5-methoxypyridine via the use of a coupling agent, such as HATU. The synthesis proceeds with an arylation followed by a decarboxylative coupling reaction. This synthetic method produces 5-iodo-2-methoxypyrimidine in high yields with excellent enantioselectivity.</p>Formula:C5H5IN2OPurity:Min. 95%Molecular weight:236.01 g/mol
