Weight | 82.106 g/mol |
---|---|
Formula | C4H6N2 |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 0 |
Aromatic Rings | 1 |
Rotatable Bonds | 0 |
1-methylimidazole (616-47-7)
1-methylimidazolium hydrogen sulfate · 1-methylimidazolium ethanoate · N-methylimidazole
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#1556 in Physics
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#4661 in Chemistry
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- Design and Magnetic Properties of a Magnetically Isolated GdIIICuII Pair. Crystal Structures of [Gd(hfa)3Cu(salen)], [Y(hfa)3Cu(salen)], [Gd(hfa)3Cu(salen)(Meim)], and [La(hfa)3(H2O)Cu(salen)] [hfa = Hexafluoroacetylacetonato, salen = N,N-Ethylenebis(salicylideneaminato), Meim = 1-Methylimidazole] (Inorganic Chemistry, 1997)
- The Hydrogen Bonding Interactions between the Ionic Liquid 1-Ethyl-3-Methylimidazolium Ethyl Sulfate and Water (Journal of Physical Chemistry B, 2010)
- Electrochemical, theoretical and XPS studies of 2-mercapto-1-methylimidazole adsorption on carbon steel in 1 M HClO4 (Applied Surface Science, 2007)
- Antiparallel side-by-side dimeric motif for sequence-specific recognition in the minor groove of DNA by the designed peptide 1-methylimidazole-2-carboxamide netropsin. (Proceedings of the National Academy of Sciences of the United States of America, 1992)
- 2-Mercapto-1-methylimidazole as corrosion inhibitor for copper in hydrochloric acid (Applied Surface Science, 2006)
- Structure of a dioxygen adduct of (1-methylimidazole)-meso-tetrakis(.alpha.,.alpha.,.alpha.,.alpha.,-o-pivalamidophenyl)porphinatoiron(II). An iron dioxygen model for the heme component of oxymyoglobin (Inorganic Chemistry, 1978)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. - H302: Harmful if swallowed
Warning Acute toxicity, oral - Category 4 - H314: Causes severe skin burns and eye damage
Danger Skin corrosion/irritation - Category 1A, B, C - 1-methylimidazolium hydrogen sulfate
- 1-methylimidazolium ethanoate
- N-methylimidazole
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SMILESCN1C=CN=C1
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InChIKeyMCTWTZJPVLRJOU-UHFFFAOYSA-N
- Pubchem - 1-methylimidazole
- Wikipedia - 1-methylimidazole
1-Methylimidazole or N-methylimidazole is an aromatic heterocyclic organic compound with the formula CH3C3H3N2. It is a colourless liquid that is used as a specialty solvent, a base, and as a precursor to some ionic liquids. It is a fundamental nitrogen heterocycle and as such mimics for various nucleoside bases as well as histidine and histamine,
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2-(Bromomethyl)-1-methyl-1H-imidazole hydrobromide
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(1-Methyl-1H-imidazol-2-yl)methanamine
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(1-Methyl-1H-imidazol-2-yl)methanol
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2-bromo-1-ethyl-1H-imidazole hydrochloride
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[2-(1H-imidazol-1-yl)propyl]amine dihydrochloride hydrate
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2-(2-Chloroethyl)-1-methyl-1H-imidazole hydrochloride
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4,5-diiodo-1-methyl-1H-imidazole
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3-(1H-imidazol-1-yl)propanoic acid
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(1-Methyl-1H-imidazol-2-yl)acetonitrile
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2-(1-Methyl-1H-imidazol-2-yl)ethanol
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5-(Chloromethyl)-1-methyl-1H-imidazole hydrochloride
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1H-Imidazol-2-amine
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{2-[(1-methyl-1H-imidazol-2-yl)thio]ethyl}amine hydrochloride
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2-(2-methyl-1H-imidazol-1-yl)ethanol
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2,5-Diiodo-1-methylimidazole
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1-(2,2-Diethoxyethyl)-1H-imidazole
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N-[(1-methyl-1H-imidazol-2-yl)methyl]propan-2-amine
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530-62-1
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2-(chloromethyl)-1-ethyl-1H-imidazole hydrochloride
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(1-Ethyl-1H-imidazol-2-yl)methanol
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1-(1-ethyl-1H-imidazol-2-yl)methanamine
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