(E)-3-(4-hydroxy-3-propyl-5-((E)-(thiazol-2-ylimino)methyl)phenyl)-1-(4-methoxy phenyl)prop-2-en-1-one

Base Information

Chemical Name:(E)-3-(4-hydroxy-3-propyl-5-((E)-(thiazol-2-ylimino)methyl)phenyl)-1-(4-methoxy phenyl)prop-2-en-1-one
CAS No.:1616108-83-8
Molecular Formula:C₂₃H₂₂N₂O₃S
Molecular Weight:406.505
Hs Code.:

Synonyms:(E)-3-(4-hydroxy-3-propyl-5-((E)-(thiazol-2-ylimino)methyl)phenyl)-1-(4-methoxy phenyl)prop-2-en-1-one

Suppliers and Price of (E)-3-(4-hydroxy-3-propyl-5-((E)-(thiazol-2-ylimino)methyl)phenyl)-1-(4-methoxy phenyl)prop-2-en-1-one

Supply Marketing:

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

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of (E)-3-(4-hydroxy-3-propyl-5-((E)-(thiazol-2-ylimino)methyl)phenyl)-1-(4-methoxy phenyl)prop-2-en-1-one

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of (E)-3-(4-hydroxy-3-propyl-5-((E)-(thiazol-2-ylimino)methyl)phenyl)-1-(4-methoxy phenyl)prop-2-en-1-one

There total 3 articles about (E)-3-(4-hydroxy-3-propyl-5-((E)-(thiazol-2-ylimino)methyl)phenyl)-1-(4-methoxy phenyl)prop-2-en-1-one 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: 66.0%

: 96-50-4
2-thiazolylamine

: 1616108-70-3
C₂₀H₂₀O₄

: 1616108-83-8
(E)-3-(4-hydroxy-3-propyl-5-((E)-(thiazol-2-ylimino)methyl)phenyl)-1-(4-methoxy phenyl)prop-2-en-1-one

Guidance literature:: In ethanol; for 3h; Reflux;
DOI:10.1016/j.ejmech.2014.05.029

Reference yield:

: 644-35-9
5-propylphenol

: 1616108-83-8
(E)-3-(4-hydroxy-3-propyl-5-((E)-(thiazol-2-ylimino)methyl)phenyl)-1-(4-methoxy phenyl)prop-2-en-1-one

Guidance literature:: Multi-step reaction with 3 steps

1.1: trifluoroacetic acid / 4 h / 120 °C

1.2: 2 h / 100 °C

2.1: hydrogenchloride / water; 1,4-dioxane / 80 - 90 °C

3.1: ethanol / 3 h / Reflux

With hydrogenchloride; trifluoroacetic acid; In 1,4-dioxane; ethanol; water; 1.1: |Duff Aldehyde Synthesis / 1.2: |Duff Aldehyde Synthesis;
DOI:10.1016/j.ejmech.2014.05.029

Reference yield:

: 1357466-05-7
4-hydroxy-5-propylisophthalaldehyde

: 100-06-1
1-(4-methoxyphenyl)ethanone

: 1616108-83-8
(E)-3-(4-hydroxy-3-propyl-5-((E)-(thiazol-2-ylimino)methyl)phenyl)-1-(4-methoxy phenyl)prop-2-en-1-one

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride / water; 1,4-dioxane / 80 - 90 °C

2: ethanol / 3 h / Reflux

With hydrogenchloride; In 1,4-dioxane; ethanol; water;
DOI:10.1016/j.ejmech.2014.05.029