1,2-Dimethyl-1H-benzimidazole is an organic compound characterized by its fused benzene and imidazole rings, which contribute to its aromatic properties. It features two methyl groups attached to the nitrogen-containing imidazole ring, specifically at the 1 and 2 positions. This substitution pattern influences its chemical reactivity and solubility. The compound is typically a white to light yellow crystalline solid, exhibiting moderate stability under standard conditions. It is soluble in organic solvents such as ethanol and dichloromethane but has limited solubility in water due to its hydrophobic nature. 1,2-Dimethyl-1H-benzimidazole is of interest in various fields, including pharmaceuticals and materials science, due to its potential biological activities and applications in synthesizing other chemical compounds. Its structure allows for interactions with biological targets, making it a subject of research in medicinal chemistry. Safety data should be consulted for handling and exposure guidelines, as with any chemical substance.

1,2-dimethyl-1H-benzimidazole

2876-08-6: 1,2-Dimethylbenzimidazole, 1H-benzimidazole, 1,2-dimethyl-, 2876-08-6

1,2-Dimethylbenzimidazole

1H-Benzimidazole, 1,2-dimethyl-

1,2-Dimethylbenzimidazole is a reactive compound that has minimal toxicity. It can be used in vitro to study the cytotoxic activity of drugs and in vivo as a probe for the activation of G proteins. 1,2-Dimethylbenzimidazole is useful for the study of cancer cells because it can be activated by UV irradiation or visible light. The photophysical properties of this compound have been investigated using nmr spectroscopy and in vitro cytotoxicity assays. The tautomers are also known to react with mercaptals, which are used as protective groups during chemical synthesis.

CAS 2876-08-6: 1,2-dimethyl-1H-benzimidazole

1,2-Dimethylbenzimidazole

Ref: 10-F633236

1H-Benzimidazole, 1,2-dimethyl-

Ref: IN-DA002WEA

1,2-Dimethylbenzimidazole

Ref: 3B-D3665

1,2-Dimethylbenzimidazole

Ref: 3D-CAA87608

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Ref: 54-OR954313