Weight | 96.089 g/mol |
---|---|
Formula | C4H4N2O |
Hydrogen Acceptors | 2 |
Hydrogen Donors | 1 |
Aromatic Rings | 1 |
Rotatable Bonds | 1 |
Imidazole-2-carboxaldehyde (10111-08-7)
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- Crystal and molecular structures of eight-coordinate (CuN4O4) and six-coordinate (CuN4O2) Cu(II) complexes with 4-methyl-5-imidazole-carboxaldehyde or 1-benzyl-2-hydroxymethylimidazole, respectively: Spectroscopic and potentiometric studies (Polyhedron, 1999)
- Synthesis, characterization and antimicrobial activity of transition metal complexes with the Schiff base derived from imidazole-2-carboxaldehyde and glycylglycine (Journal of Coordination Chemistry, 2009)
- Synthesis of 1-(dimethylsulfamoyl)-2- and 5-imidazolecarboxaldehydes. Rearrangement of 1-(dimethylsulfamoyl)-5-imidazole-carboxaldehyde to the 4-carboxaldehyde (Journal of Heterocyclic Chemistry, 1995)
- The role of the side group in reactions involving 1-propyl-2-methylimidazole and 1-propyl-2-imidazole-carboxaldehyde and Co(II), Ni(II), Cu(II) and Zn(II) ions (Polish Journal of Chemistry, 1999)
- IMPROVED SYNTHESIS OF IMIDAZOLE-2-CARBOXALDEHYDE, IMIDAZOLE-2-CARBOXYLIC ACID, AND ETHYL IMIDAZOLE-2-CARBOXYLATE (Journal of Organic Chemistry, 1995)
- A Convenient Synthesis of 2-Butyl-4(5)-chloro-1H-imidazole-5(4)-carboxaldehyde (Synthetic Communications, 1992)
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Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC1=CN=C(N1)C=O
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InChIKeyXYHKNCXZYYTLRG-UHFFFAOYSA-N
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