methyl (E)-4-(3-(7-hydroxy-2-oxo-2H-chromen-3-yl)-3-oxoprop-1-en-1-yl)benzoate

Base Information

Chemical Name:methyl (E)-4-(3-(7-hydroxy-2-oxo-2H-chromen-3-yl)-3-oxoprop-1-en-1-yl)benzoate
CAS No.:1470057-49-8
Molecular Formula:C₂₀H₁₄O₆
Molecular Weight:350.328
Hs Code.:

Synonyms:methyl (E)-4-(3-(7-hydroxy-2-oxo-2H-chromen-3-yl)-3-oxoprop-1-en-1-yl)benzoate

Suppliers and Price of methyl (E)-4-(3-(7-hydroxy-2-oxo-2H-chromen-3-yl)-3-oxoprop-1-en-1-yl)benzoate

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 methyl (E)-4-(3-(7-hydroxy-2-oxo-2H-chromen-3-yl)-3-oxoprop-1-en-1-yl)benzoate

Chemical Property:

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

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Technology Process of methyl (E)-4-(3-(7-hydroxy-2-oxo-2H-chromen-3-yl)-3-oxoprop-1-en-1-yl)benzoate

There total 2 articles about methyl (E)-4-(3-(7-hydroxy-2-oxo-2H-chromen-3-yl)-3-oxoprop-1-en-1-yl)benzoate 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%

: 10441-27-7
3-acetyl-7-hydroxy-chromen-2-one

: 1571-08-0
methyl 4-formylbenzoate

: 1470057-49-8
methyl (E)-4-(3-(7-hydroxy-2-oxo-2H-chromen-3-yl)-3-oxoprop-1-en-1-yl)benzoate

Guidance literature:: With piperidine; In ethanol; Reflux;
DOI:10.1016/j.ejmech.2013.07.014

Reference yield:

: 95-01-2
2,4-Dihydroxybenzaldehyde

: 1470057-49-8
methyl (E)-4-(3-(7-hydroxy-2-oxo-2H-chromen-3-yl)-3-oxoprop-1-en-1-yl)benzoate

Guidance literature:: Multi-step reaction with 2 steps

1: piperidine / ethanol / 50 °C

2: piperidine / ethanol / Reflux

With piperidine; In ethanol;
DOI:10.1016/j.ejmech.2013.07.014