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Assay
98%
bp
70-74 °C/1 mmHg (lit.)
mp
36-39 °C (lit.)
SMILES string
[H]C(=O)c1nccn1C
InChI
1S/C5H6N2O/c1-7-3-2-6-5(7)4-8/h2-4H,1H3
InChI key
UEBFLTZXUXZPJO-UHFFFAOYSA-N
Related Categories
General description
1-Methyl-2-imidazolecarboxaldehyde is a heterocyclic building block. It affords tripodal ligands on condensation reaction with tris-(2-aminoethyl)amine (tren). These tripodal ligands react with iron(III) salts in the presence of air to afford iron(II) complexes. Its vibrational spectral studies have been reported.
Application
1-Methyl-2-imidazolecarboxaldehyde may be used in the synthesis of:
- Schiff bases
- ligand N,N-dimethyl-N′-(1-methylimidazole-2-ylmethyl)-ethylenediamine
- [(bis(1-methylimidazol-2-yl)methyl)(2-(pyridyl-2-yl)ethyl)amine]
Signal Word
Warning
Hazard Statements
Precautionary Statements
Hazard Classifications
Eye Irrit. 2 - Skin Irrit. 2 - STOT SE 3
Target Organs
Respiratory system
Storage Class Code
11 - Combustible Solids
WGK
WGK 3
Flash Point(F)
215.6 °F - closed cup
Flash Point(C)
102 °C - closed cup
Personal Protective Equipment
dust mask type N95 (US), Eyeshields, Gloves
Certificates of Analysis (COA)
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Synthesis and characterization of tripodal iron (II) complexes prepared from 2-pyridinecarboxaldehyde and 1-methyl-2-imidazolecarboxaldehyde: stabilization of iron (II) cations with N 6 donor sets.
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DFT, FT-IR and FT-Raman investigations of 1-methyl-2-imidazolecarboxaldehyde.
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