1,2,4-triphenyl-1H-imidazole-5-carbaldehyde

Base Information

Chemical Name:1,2,4-triphenyl-1H-imidazole-5-carbaldehyde
CAS No.:1345509-77-4
Molecular Formula:C₂₂H₁₆N₂O
Molecular Weight:324.382
Hs Code.:

Synonyms:1,2,4-triphenyl-1H-imidazole-5-carbaldehyde

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of 1,2,4-triphenyl-1H-imidazole-5-carbaldehyde

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Technology Process of 1,2,4-triphenyl-1H-imidazole-5-carbaldehyde

There total 6 articles about 1,2,4-triphenyl-1H-imidazole-5-carbaldehyde which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 88.0%

: 820975-55-1
α-azidocinnamaldehyde

: 1137-96-8,26505-49-7,201024-81-9
N-(benzylidene)aniline N-oxide

: 1345509-77-4
1,2,4-triphenyl-1H-imidazole-5-carbaldehyde

Guidance literature:: With magnesium sulfate; In 1,2-dichloro-ethane; at 66 ℃; for 48h; Inert atmosphere;
DOI:10.1021/ol202650z

Reference yield: 82.0%

: 104-55-2
3-phenyl-propenal

: 1527-91-9
N-phenylbenzamidine

: 1345509-77-4
1,2,4-triphenyl-1H-imidazole-5-carbaldehyde

Guidance literature:: With 1,10-Phenanthroline; iron(III) chloride hexahydrate; iodine; In 1,2-dichloro-benzene; at 110 ℃; for 18h; regioselective reaction;
DOI:10.1002/adsc.201500701

Reference yield: 78.0%

: 2579-22-8
Phenylpropargyl aldehyde

: 1527-91-9
N-phenylbenzamidine

: 1345509-77-4
1,2,4-triphenyl-1H-imidazole-5-carbaldehyde

Guidance literature:: With oxygen; silver trifluoromethanesulfonate; acetic acid; In water; dimethyl sulfoxide; at 120 ℃; for 10h; Reagent/catalyst; Solvent; regioselective reaction; Catalytic behavior; Sealed tube; Schlenk technique;
DOI:10.1039/c7ob01242j