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Atomfair 1-(triphenylmethyl)-1H-imidazole-4-carbaldehyde C23H18N2O

Description 1-(Triphenylmethyl)-1H-imidazole-4-carbaldehyde (CAS No. 33016-47-6) is a high-purity organic compound with the molecular formula C23H18N2O , widely utilized in synthetic chemistry and pharmaceutical research. This compound features a trityl-protected imidazole core with a reactive aldehyde functional group, making it a versatile building block for heterocyclic synthesis, ligand design, and medicinal chemistry applications. Its robust trityl group enhances stability during complex reactions while allowing selective deprotection when required. Suitable for use in nucleophilic additions, cross-coupling reactions, and as a precursor for imidazole-based scaffolds. Provided as a crystalline solid with ??95% purity (HPLC), rigorously tested for consistency and stored under inert conditions…

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Description

Description

1-(Triphenylmethyl)-1H-imidazole-4-carbaldehyde (CAS No. 33016-47-6) is a high-purity organic compound with the molecular formula C23H18N2O, widely utilized in synthetic chemistry and pharmaceutical research. This compound features a trityl-protected imidazole core with a reactive aldehyde functional group, making it a versatile building block for heterocyclic synthesis, ligand design, and medicinal chemistry applications. Its robust trityl group enhances stability during complex reactions while allowing selective deprotection when required. Suitable for use in nucleophilic additions, cross-coupling reactions, and as a precursor for imidazole-based scaffolds. Provided as a crystalline solid with ??95% purity (HPLC), rigorously tested for consistency and stored under inert conditions to ensure optimal performance.

  • CAS No: 33016-47-6
  • Molecular Formula: C23H18N2O
  • Molecular Weight: 338.4
  • Exact Mass: 338.141913202
  • Monoisotopic Mass: 338.141913202
  • IUPAC Name: 1-tritylimidazole-4-carbaldehyde
  • SMILES: C1=CC=C(C=C1)C(C2=CC=CC=C2)(C3=CC=CC=C3)N4C=C(N=C4)C=O
  • Synonyms: 1-(triphenylmethyl)-1H-imidazole-4-carbaldehyde, 620-447-0, 33016-47-6, 1-Tritylimidazole-4-carboxaldehyde, 1-Trityl-1H-imidazole-4-carbaldehyde

Application

1-(Triphenylmethyl)-1H-imidazole-4-carbaldehyde serves as a key intermediate in the synthesis of imidazole derivatives for pharmaceutical and agrochemical applications. Its aldehyde group enables facile condensation reactions to form Schiff bases or heterocyclic fused systems. Researchers employ this compound in the development of enzyme inhibitors, metal-organic frameworks (MOFs), and fluorescent probes due to its tunable electronic properties. The trityl group offers steric protection during multi-step syntheses, particularly in peptide and nucleoside modifications.

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