CAS 882562-56-3
:1-(2,5-Dichloro-4-pyrimidinyl)-1H-benzimidazole
Description:
1-(2,5-Dichloro-4-pyrimidinyl)-1H-benzimidazole is a chemical compound characterized by its unique structure, which combines a benzimidazole moiety with a pyrimidine ring substituted with chlorine atoms. This compound typically exhibits properties such as moderate solubility in organic solvents and limited solubility in water, which is common for many heterocyclic compounds. The presence of chlorine substituents often enhances the compound's biological activity and can influence its reactivity and stability. It may be utilized in various applications, including pharmaceuticals, agrochemicals, or as a research chemical, owing to its potential as a bioactive agent. The compound's molecular structure allows for interactions with biological targets, making it of interest in medicinal chemistry. Additionally, its synthesis may involve standard organic reactions, including halogenation and cyclization processes. Safety and handling precautions are essential, as with many chemical substances, due to potential toxicity or environmental impact.
Formula:C11H6Cl2N4
InChI:InChI=1S/C11H6Cl2N4/c12-7-5-14-11(13)16-10(7)17-6-15-8-3-1-2-4-9(8)17/h1-6H
InChI key:InChIKey=IXRXAUUILFDWTP-UHFFFAOYSA-N
SMILES:ClC=1C(N2C=3C(N=C2)=CC=CC3)=NC(Cl)=NC1
Synonyms:- 1-(2,5-Dichloropyrimidin-4-yl)benzimidazole
- 1-(2,5-Dichloropyrimidin-4-yl)-1H-benzo[d]imidazole
- 1-(2,5-Dichloropyrimidin-4-yl)-1H-benzimidazole
- 1H-Benzimidazole, 1-(2,5-dichloro-4-pyrimidinyl)-
- 1-(2,5-Dichloro-4-pyrimidinyl)-1H-benzimidazole
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