3-Butenoic acid, 2-oxo-4-phenyl-, potassium salt, (E)-

Base Information

Chemical Name:3-Butenoic acid, 2-oxo-4-phenyl-, potassium salt, (E)-
CAS No.:140653-89-0
Molecular Formula:C10H8O3.K
Molecular Weight:214.262
Hs Code.:

Synonyms:

Suppliers and Price of 3-Butenoic acid, 2-oxo-4-phenyl-, potassium salt, (E)-

Supply Marketing:

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

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Chemical Property of 3-Butenoic acid, 2-oxo-4-phenyl-, potassium salt, (E)-

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of 3-Butenoic acid, 2-oxo-4-phenyl-, potassium salt, (E)-

There total 2 articles about 3-Butenoic acid, 2-oxo-4-phenyl-, potassium salt, (E)- 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: 95.0%

: 100-52-7
benzaldehyde

: 127-17-3
2-oxo-propionic acid

: 140653-89-0
(E)-benzylideneglyoxylic acid potassium salt

Guidance literature:: With potassium hydroxide; In methanol; at 0 - 40 ℃;
DOI:10.1002/adsc.201701413

Reference yield:

: 100-52-7
benzaldehyde

: 127-17-3
2-oxo-propionic acid

: potassium hydroxide

: 140653-89-0
(E)-benzylideneglyoxylic acid potassium salt

Guidance literature:: In methanol; at 10 - 40 ℃; Inert atmosphere; Schlenk technique;
DOI:10.1021/om300896z

Reference yield: 93.0%

: 140653-89-0
(E)-benzylideneglyoxylic acid potassium salt

: 123-54-6,81235-32-7
acetylacetone

: 1313870-25-5
(R)-5-acetyl-6-methyl-4-phenyl-3,4-dihydro-2H-pyran-2-one

Guidance literature:: With C₂₀H₂₀N₃O₃⁽¹⁺⁾*Cl^(1-); sodium acetate; lithium chloride; In 1,4-dioxane; at 20 ℃; for 40h; Reagent/catalyst; Solvent; Time; enantioselective reaction; Sealed tube; Schlenk technique;
DOI:10.1002/adsc.201701413