2-[4-(1,3-benzodioxol-5-yloxy)benzylidene]-N-(4-methoxyphenyl)hydrazinecarbothioamide

Base Information

Chemical Name:2-[4-(1,3-benzodioxol-5-yloxy)benzylidene]-N-(4-methoxyphenyl)hydrazinecarbothioamide
CAS No.:1444851-57-3
Molecular Formula:C₂₂H₁₉N₃O₄S
Molecular Weight:421.477
Hs Code.:

Synonyms:2-[4-(1,3-benzodioxol-5-yloxy)benzylidene]-N-(4-methoxyphenyl)hydrazinecarbothioamide

Suppliers and Price of 2-[4-(1,3-benzodioxol-5-yloxy)benzylidene]-N-(4-methoxyphenyl)hydrazinecarbothioamide

Supply Marketing:

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

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Total 1 raw suppliers

Chemical Property of 2-[4-(1,3-benzodioxol-5-yloxy)benzylidene]-N-(4-methoxyphenyl)hydrazinecarbothioamide

Chemical Property:

Purity/Quality:: 98% ^*data from raw suppliers

Safty Information:

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Technology Process of 2-[4-(1,3-benzodioxol-5-yloxy)benzylidene]-N-(4-methoxyphenyl)hydrazinecarbothioamide

There total 4 articles about 2-[4-(1,3-benzodioxol-5-yloxy)benzylidene]-N-(4-methoxyphenyl)hydrazinecarbothioamide 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: 68.0%

: 40207-03-2
p-Anisidinothioformyl-hydrazin

: 169943-89-9
4-(3.4-Methylenedioxyphenoxy)-benzaldehyde

: 1444851-57-3
2-[4-(1,3-benzodioxol-5-yloxy)benzylidene]-N-(4-methoxyphenyl)hydrazinecarbothioamide

Guidance literature:: With acetic acid; In ethanol; Reflux;
DOI:10.1016/j.ejmech.2013.04.019

Reference yield:

: 104-94-9
4-methoxy-aniline

: 1444851-57-3
2-[4-(1,3-benzodioxol-5-yloxy)benzylidene]-N-(4-methoxyphenyl)hydrazinecarbothioamide

Guidance literature:: Multi-step reaction with 2 steps

1.1: sodium hydroxide / N,N-dimethyl-formamide / 1 h / 20 - 35 °C

1.2: 1 h / 60 - 70 °C

2.1: acetic acid / ethanol / Reflux

With acetic acid; sodium hydroxide; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2013.04.019

Reference yield:

: 459-57-4
4-fluorobenzaldehyde

: 1444851-57-3
2-[4-(1,3-benzodioxol-5-yloxy)benzylidene]-N-(4-methoxyphenyl)hydrazinecarbothioamide

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / N,N-dimethyl-formamide / Reflux

2: acetic acid / ethanol / Reflux

With potassium carbonate; acetic acid; In ethanol; N,N-dimethyl-formamide;
DOI:10.1016/j.ejmech.2013.04.019