Butanoic acid, 3-oxo-2-(phenylhydrazono)-, phenylmethyl ester

Base Information

Chemical Name:Butanoic acid, 3-oxo-2-(phenylhydrazono)-, phenylmethyl ester
CAS No.:111033-07-9
Molecular Formula:C17H16N2O3
Molecular Weight:296.32100
Hs Code.:
Mol file:111033-07-9.mol

Synonyms:3-Oxo-2-phenylhydrazono-buttersaeure-benzylester;benzyl 3-oxo-2-(2-phenylhydrazono)butanoate;benzyl 2,3-dioxobutanoate-2-phenylhydrazone;3-oxo-2-phenylhydrazono-butyric acid benzyl ester;Butanoic acid,3-oxo-2-(phenylhydrazono)-,phenylmethyl ester;

Suppliers and Price of Butanoic acid, 3-oxo-2-(phenylhydrazono)-, phenylmethyl ester

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 Butanoic acid, 3-oxo-2-(phenylhydrazono)-, phenylmethyl ester

Chemical Property:

PSA：67.76000
LogP:2.85990

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:: SDS file from LookChem

Useful:

Technology Process of Butanoic acid, 3-oxo-2-(phenylhydrazono)-, phenylmethyl ester

There total 3 articles about Butanoic acid, 3-oxo-2-(phenylhydrazono)-, phenylmethyl ester 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: 91.0%

: 5396-89-4
benzyl acetoacetate

: 62-53-3
aniline

: 111033-07-9
benzyl 2,3-dioxobutanoate-2-phenylhydrazone

Guidance literature:: aniline; With hydrogenchloride; sodium nitrite; In water; salt/ice cooling;

benzyl acetoacetate; With sodium acetate; In ethanol; water; at 0 - 20 ℃; for 1.5h;
DOI:10.1016/S0040-4020(97)10288-5