CAS 1407521-91-8
:2-Chloro-3-iodo-5-methyl-1,6-naphthyridine
Description:
2-Chloro-3-iodo-5-methyl-1,6-naphthyridine is a heterocyclic organic compound characterized by its naphthyridine structure, which consists of a fused bicyclic system containing nitrogen atoms. This compound features a chlorine atom at the 2-position, an iodine atom at the 3-position, and a methyl group at the 5-position of the naphthyridine ring. The presence of halogen substituents (chlorine and iodine) can significantly influence its reactivity and potential applications in medicinal chemistry, particularly in the development of pharmaceuticals. The methyl group contributes to the compound's hydrophobic characteristics, which may affect its solubility and biological activity. Additionally, the unique arrangement of atoms in this compound may impart specific electronic properties, making it a candidate for various chemical reactions, including nucleophilic substitutions and coupling reactions. Overall, 2-Chloro-3-iodo-5-methyl-1,6-naphthyridine is of interest in research fields focused on drug discovery and synthesis of complex organic molecules.
Formula:C9H6ClIN2
InChI:InChI=1S/C9H6ClIN2/c1-5-6-4-7(11)9(10)13-8(6)2-3-12-5/h2-4H,1H3
InChI key:InChIKey=SIQXQAGZZMBTNP-UHFFFAOYSA-N
SMILES:CC=1C2=C(N=C(Cl)C(I)=C2)C=CN1
Synonyms:- 1,6-Naphthyridine, 2-chloro-3-iodo-5-methyl-
- 2-Chloro-3-iodo-5-methyl-1,6-naphthyridine
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2-Chloro-3-iodo-5-methyl-1,6-naphthyridine
CAS:2-Chloro-3-iodo-5-methyl-1,6-naphthyridinePurity:≥95%Molecular weight:304.51g/mol
