1-Methyl-2-imidazolecarboxaldehyde Chemical Properties

Melting point:

36-39 °C (lit.)

Boiling point:

70-74 °C/1 mmHg (lit.)

Density 

1.2111 (rough estimate)

refractive index 

1.5090 (estimate)

Flash point:

215 °F

storage temp. 

under inert gas (nitrogen or Argon) at 2-8°C

pka

4.17±0.25(Predicted)

form 

Liquid

color 

Clear colorless to yellow

Water Solubility 

Soluble in water.

Sensitive 

Air Sensitive

InChI

InChI=1S/C5H6N2O/c1-7-3-2-6-5(7)4-8/h2-4H,1H3

InChIKey

UEBFLTZXUXZPJO-UHFFFAOYSA-N

SMILES

C1(C=O)N(C)C=CN=1

CAS DataBase Reference

13750-81-7(CAS DataBase Reference)

NIST Chemistry Reference

1H-imidazole-2-carboxaldehyde, 1-methyl-(13750-81-7)

Safety Information

Hazard Codes 

Xi

Risk Statements 

36/37/38

Safety Statements 

26-36-37/39

WGK Germany 

3

HazardClass 

IRRITANT

HS Code 

29339900

MSDS

• Language:English Provider:SigmaAldrich
• Language:English Provider:ACROS

1-Methyl-2-imidazolecarboxaldehyde Usage And Synthesis

Chemical Properties

White to yellow crystalline mass,

Uses

It is an important raw material and intermediate used in organic synthesis, Pharmaceuticals, agrochemicals and dyestuffs.

Uses

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]

Synthesis Reference(s)

Journal of Medicinal Chemistry, 26, p. 121, 1983 DOI: 10.1021/jm00356a001

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.

Synthesis

A THF solution of n-butyllithium (nBuLi) was added slowly and dropwise to an anhydrous THF (100 mL) solution of 1-methylimidazole (8.2 g, 100 mmol) cooled to -70 °C. The reaction temperature was maintained at -70 °C and after stirring for 30 min, freshly distilled N,N-dimethylformamide (DMF, 7.3 g, 100 mmol) was added. The reaction mixture was continued to be stirred at 0 °C for 2 h. The reaction was subsequently quenched with ice water. The mixture was extracted with ethyl acetate (EtOAc), the organic phases were combined and dried over anhydrous sodium sulfate (Na2SO4). After evaporation of the solvent under reduced pressure, an oily residue was obtained, which was further purified by distillation under reduced pressure to afford the target product 1-methyl-1H-imidazole-2-carbaldehyde in 68% yield. The structure of the product was confirmed by 1H-NMR (CDCl3): δ 9.76 (s, 1H, CHO), 7.22 (s, 1H, Im-CH), 7.07 (s, 1H, Im-CH), 3.96 (s, 3H, CH3). High-resolution mass spectrometry (EI-HRMS) analysis results: m/z calculated value C5H6N2O 110.0480, measured value 110.0481 (100%), 82.0493 (60%).

References

[1] Inorganica Chimica Acta, 2011, vol. 375, # 1, p. 213 - 219
[2] Dalton Transactions, 2015, vol. 44, # 17, p. 8013 - 8020
[3] Chemistry - A European Journal, 2015, vol. 21, # 36, p. 12735 - 12740
[4] Dalton Transactions, 2011, vol. 40, # 40, p. 10416 - 10433
[5] Tetrahedron, 2000, vol. 56, # 4, p. 645 - 657

1-Methyl-2-imidazolecarboxaldehyde(13750-81-7)Related Product Information

• Tribenuron methyl
• Imidazole
• Pirimiphos-methyl
• Methyl acetate
• Imidazole-2-carboxaldehyde
• METSULFURON METHYL
• p-Tolualdehyde
• 4-(Trifluoromethyl)benzaldehyde
• 1H-Imidazole-4-carbaldehyde
• Methyl salicylate
• 1-Methylimidazole
• Kresoxim-methyl
• Thiophanate-methyl
• Methyl
• 1-METHYL-2-FORMYLBENZIMIDAZOLE
• Methyl bromide
• 1-Tritylimidazole-4-carboxaldehyde
• Parathion-methyl