CAS 78607-36-0
:2-Chloro-3-iodopyridine
Description:
2-Chloro-3-iodopyridine is a heterocyclic organic compound characterized by the presence of both chlorine and iodine substituents on a pyridine ring. The molecular structure consists of a six-membered aromatic ring containing five carbon atoms and one nitrogen atom, with chlorine attached to the second carbon and iodine to the third carbon of the ring. This compound typically appears as a colorless to pale yellow liquid or solid, depending on its physical state at room temperature. It is known for its reactivity, particularly in nucleophilic substitution reactions, due to the presence of the halogen atoms, which can influence its chemical behavior. 2-Chloro-3-iodopyridine is often utilized in organic synthesis, particularly in the development of pharmaceuticals and agrochemicals, owing to its ability to serve as an intermediate in various chemical reactions. Additionally, it may exhibit biological activity, making it of interest in medicinal chemistry. Proper handling and storage are essential, as with many halogenated compounds, due to potential toxicity and environmental concerns.
Formula:C5H3ClIN
InChI:InChI=1/C5H3ClIN/c6-5-4(7)2-1-3-8-5/h1-3H
SMILES:c1cc(c(Cl)nc1)I
Synonyms:- Buttpark 34\07-77
- 3-Iodo-2-Chloropyridine
- 2-Choro-3-Iodopyridine
- 2-Chloro-3-Indopyridine
- 2-Chloro-3-iodopyridine, 98+%
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Found 6 products.
2-Chloro-3-iodopyridine
CAS:<p>2-Chloro-3-iodopyridine</p>Formula:C5H3ClINPurity:≥95%Color and Shape: faint yellow crystalline solidMolecular weight:239.44g/mol2-Chloro-3-iodopyridine
CAS:Formula:C5H3ClINPurity:>98.0%(GC)Color and Shape:White to Light yellow to Light orange powder to crystalMolecular weight:239.442-Chloro-3-iodopyridine
CAS:Controlled Product<p>Applications 2-Chloro-3-iodopyridine (cas# 78607-36-0) is a compound useful in organic synthesis.<br></p>Formula:C5H3ClINColor and Shape:NeatMolecular weight:239.442-Chloro-3-iodopyridine
CAS:<p>2-Chloro-3-iodopyridine is an efficient method for the synthesis of various 2-chloro-3-iodopyridines. The reaction is catalyzed by triphosgene, a reagent that is also used in the synthesis of other important heterocycles. In this process, triphosgene reacts with a broad range of primary amines to form chloronitroso derivatives. These compounds are then used to synthesize 2-chloro-3-iodopyridines by reaction with pyridine. The reaction can be run at temperatures as low as -78°C, which has led to its use in bladder cancer research and some other reactions involving aminations or furopyridines.</p>Formula:C5H3ClINPurity:Min. 95%Molecular weight:239.44 g/mol





