CAS 4344-61-0
:1H-Benzimidazole,1-methyl-2-(methylthio)-
Description:
1H-Benzimidazole, 1-methyl-2-(methylthio)- is an organic compound characterized by its benzimidazole core, which consists of a fused benzene and imidazole ring. This compound features a methyl group at the 1-position and a methylthio group at the 2-position of the benzimidazole ring. It is typically a white to off-white solid, exhibiting moderate solubility in polar organic solvents. The presence of the methylthio group imparts unique chemical reactivity, making it of interest in various synthetic applications, particularly in medicinal chemistry and material science. The compound may exhibit biological activity, potentially influencing its use in pharmaceuticals. Its molecular structure allows for interactions with biological targets, which can be explored for therapeutic purposes. As with many organic compounds, safety data should be consulted, as it may pose hazards if not handled properly. Overall, 1H-Benzimidazole, 1-methyl-2-(methylthio)- is a versatile compound with potential applications in various fields of chemistry.
Formula:C9H10N2S
Synonyms:- Benzimidazole,1-methyl-2-(methylthio)- (6CI,7CI)
- 1-Methyl-2-(methylthio)benzimidazole
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Found 2 products.
1-Methyl-2-(methylthio)-1H-benzo[d]imidazole
CAS:1-Methyl-2-(methylthio)-1H-benzo[d]imidazolePurity:95%Molecular weight:178.26g/mol1-Methyl-2-(methylsulfanyl)-1H-1,3-benzodiazole
CAS:<p>1-Methyl-2-(methylsulfanyl)-1H-1,3-benzodiazole is an alkylating agent that undergoes a regiospecific reaction with N-methylmorpholine and dimethylformamide to produce the desired 1-(methylsulfanyl)benzene. This process can be carried out in the presence of activated carbon to remove any byproducts. The kinetics of the reaction are dependent on temperature, which can be adjusted by using different solvents. The product is then purified through techniques such as recrystallization or distillation.</p>Formula:C9H10N2SPurity:Min. 95%Molecular weight:178.26 g/mol

