N-[1-(4-Methoxy-phenyl)-meth-(E)-ylidene]-N'-[1-phenyl-meth-(E)-ylidene]-hydrazine

Base Information

Chemical Name:N-[1-(4-Methoxy-phenyl)-meth-(E)-ylidene]-N'-[1-phenyl-meth-(E)-ylidene]-hydrazine
CAS No.:41097-54-5
Molecular Formula:C₁₅H₁₄N₂O
Molecular Weight:238.289
Hs Code.:

Synonyms:N-[1-(4-Methoxy-phenyl)-meth-(E)-ylidene]-N'-[1-phenyl-meth-(E)-ylidene]-hydrazine

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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 N-[1-(4-Methoxy-phenyl)-meth-(E)-ylidene]-N'-[1-phenyl-meth-(E)-ylidene]-hydrazine

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Technology Process of N-[1-(4-Methoxy-phenyl)-meth-(E)-ylidene]-N'-[1-phenyl-meth-(E)-ylidene]-hydrazine

There total 3 articles about N-[1-(4-Methoxy-phenyl)-meth-(E)-ylidene]-N'-[1-phenyl-meth-(E)-ylidene]-hydrazine 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: 85.0%

: 72531-34-1
C₂₂H₂₄N₂O₄S

: 41097-54-5
N-[1-(4-Methoxy-phenyl)-meth-(E)-ylidene]-N'-[1-phenyl-meth-(E)-ylidene]-hydrazine

Guidance literature:: With formic acid; In dichloromethane; for 24h; Ambient temperature;
DOI:10.1055/s-1983-30562

Reference yield: 48.0%

: 105336-81-0
4(C₅H₅)^(1-)*2Zr⁽⁴⁺⁾*2(NNCHC₆H₄OCH₃)^(2-)=((C₅H₅)2ZrNNCHC₆H₄OCH₃)2

: 100-52-7
benzaldehyde

: 1694-19-5
p-methoxystilbene

: 41097-54-5
N-[1-(4-Methoxy-phenyl)-meth-(E)-ylidene]-N'-[1-phenyl-meth-(E)-ylidene]-hydrazine

Guidance literature:: In 1,4-dioxane; benzene-d6; Aldehyde was added into a NMR tube containing a soln. of complex in C6D6 with dioxane as an internal standard at 10°C, reaction was detected over 6 h;; detected by NMR spectroscopy, yield of products was determined by gas chromatography;; Kinetics;
DOI:10.1021/om00145a030