| CAS ID | 1739-84-0 |
|---|---|
| IUPAC Name | 1,2-dimethylimidazole |
| Molecular Formula | C5H8N2 |
| Molecular Weight | |
| SMILES | CC1=NC=CN1C |
| CAS ID | 1739-84-0 |
|---|---|
| IUPAC Name | 1,2-dimethylimidazole |
| Molecular Formula | C5H8N2 |
| Molecular Weight | |
| SMILES | CC1=NC=CN1C |
| 15617 |
Synonym: 1,2-dimethyl-1h-imidazole, 1h-imidazole, 1,2-dimethyl, imidazole, 1,2-dimethyl, 1h-imidazole, dimethyl, unii-q41bc3grjb, q41bc3grjb, lupragen r dmi, 1,2-dimethylimdazole, 1,2 dimethylimidazole, n,2-dimethylimidazole
| Color | White-Yellow |
| Boiling Point | 205°C |
| UN Number | 3263 |
| Formula Weight | 96.13 |
| Physical Form | Crystal-Lump at 20°C |
| Chemical Name or Material | 1,2-Dimethylimidazole |
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An organic molecule with a five-membered imidazole ring replaced by two methyl groups is 1,2-dimethylimidazole. Its stability and reactivity make it quite popular in pharmaceuticals and chemical synthesis.
The 1,2-dimethylimidazole structure consists of an imidazole ring joined at positions 1 and 2 with methyl groups attached. Its electronic characteristics are influenced by this molecular arrangement, which makes it useful for activities like polymerization and catalysis.
Solubility of 1,2-dimethylimidazole varies with different solvents. Though it has low solubility in non-polar solvents, it is very soluble in polar organic solvents such as methanol and ethanol. Its solubility properties help it to be valuable in many kinds of chemical compositions.
Among its applications are those as a stabilizer in specialty chemicals, an intermediary in pharmaceutical synthesis, and a catalyst in polyurethane manufacturing. It also finds use in advanced material research and resin production.
Its catalytic effectiveness, solubility profile, and stability make 1,2-dimethylimidazole essential for industrial uses. It helps pharmaceutical synthesis, advances chemical formulation performance in many different fields, and boosts polymerization techniques.
