Imidazole based anticancer drug find applications in cancer chemotherapy. 3034-50-2, formula is C4H4N2O, Name is Imidazole-4-carbaldehyde. It is used as buffer component for purification of the histidine tagged recombinant proteins in immobilized metal-affinity chromatography (IMAC). Recommanded Product: Imidazole-4-carbaldehyde.
Tanaka, Tsubasa;Sunatsuki, Yukinari;Suzuki, Takayoshi research published 《 Synthesis and magnetic properties of tetrahedral tetranuclear iron(II) complexes with bis(bidentate)-type Schiff bases containing imidazole groups》, the research content is summarized as follows. Two new tetranuclear iron(II) complexes, [Fe4(H2LH)6](ClO4)8 (1ClO4: H2LH = N,N’-bis(imidazole-4-ylmethylidene)-1.4-diaminobenzene) and [Fe4(H2LMe)6](BF4)8 (2BF4: H2LMe = N,N’-bis(5-methylimidazole-4-ylmethylidene)-1.4-diaminobenzene), were synthesized from Fe(ClO4 or BF4)2·6H2O, 1.4-diaminobenzene and 4-formylimidazole or 5-methyl-4-formylimidazole. X-ray anal. revealed that these complexes have a tetrahedral structure with four iron(II) ions at the apexes and the bridging bis(bidentate) ligands on the edges. The internal space of the tetrahedron was filled with the phenylene segments of the bridging ligands. Magnetic susceptibility studies indicated that both 1ClO4 and 2BF4 showed gradual but incomplete spin-crossover (SCO) behavior, because the densely packed tetrahedral structure could prevent the contraction of the Fe-N bonds on the high-spin to low-spin transition.
Recommanded Product: Imidazole-4-carbaldehyde, 1H-Imidazole-4-carbaldehyde, also known as 1H-Imidazole-4-carbaldehyde, is a useful research compound. Its molecular formula is C4H4N2O and its molecular weight is 96.09 g/mol. The purity is usually 95%.
The starting material for a practical synthesis of a potent C17,20-lyase inhibitor. The lyase is a key enzyme in androgen biosynthesis as well as a target for treatment of androgen-dependent prostate cancer. Used to synthesize potent antimalarial drug.
1H-Imidazole-4-carbaldehyde is a chemical compound that has been shown to bind to the glucocorticoid receptor. It was synthesized by reacting 1,2-diaminobenzene with formaldehyde and then hydrolyzing the intermediate imidazolium salt, which is stable in acidic solutions. The complex can be prepared by mixing two solutions of imidazole and trifluoroacetic acid. The ligand has a redox potential of -0.1 V (vs NHE). This means it can be oxidized to the carbonyl group or reduced back to the imidazole ring. The compound is stable in neutral solution and forms stable complexes with metal ions such as Cu+, Fe3+, and Zn2+. It also coordinates well with oxygen atoms, nitrogen atoms, and water molecules. 1H-Imidazole-4-carbaldehyde has been shown to bind to glucocortic, 3034-50-2.
Referemce:
Imidazole – Wikipedia,
Imidazole | C3H4N2 – PubChem