E-2-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyimino]-2-(pyridine-1-oxide-3-yl)acetic acid

Base Information

Chemical Name:E-2-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyimino]-2-(pyridine-1-oxide-3-yl)acetic acid
CAS No.:250601-34-4
Molecular Formula:C₂₅H₂₁N₃O₆
Molecular Weight:459.458
Hs Code.:

Synonyms:E-2-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyimino]-2-(pyridine-1-oxide-3-yl)acetic acid

Suppliers and Price of E-2-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyimino]-2-(pyridine-1-oxide-3-yl)acetic acid

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-2-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyimino]-2-(pyridine-1-oxide-3-yl)acetic acid

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of E-2-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyimino]-2-(pyridine-1-oxide-3-yl)acetic acid

There total 7 articles about E-2-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyimino]-2-(pyridine-1-oxide-3-yl)acetic acid 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: 52.0%

: 64741-01-1
m-chloroperoxybenzoic acid

: 250601-30-0
ethyl E-2-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyimino]-2-(pyridin-3-yl)acetate

: 914771-42-9
methanol ethyl acetate

: 250601-34-4
E-2-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyimino]-2-(pyridine-1-oxide-3-yl)acetic acid

Guidance literature:: With hydrogenchloride; sodium hydroxide; sodium chloride; potassium carbonate; sodium thiosulfate; In tetrahydrofuran; tetrahydrofuran (10 ml)-methanol;

Reference yield:

: 250602-53-0
4-{[4-(chloromethyl)phenoxy]methyl}-5-methyl-2-phenyl-1,3-oxazole

: 250601-34-4
E-2-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyimino]-2-(pyridine-1-oxide-3-yl)acetic acid

Guidance literature:: Multi-step reaction with 2 steps

1: hydrogenchloride; sodium chloride; sodium hydrogencarbonate / N,N-dimethyl-formamide

2: hydrogenchloride; sodium hydroxide; sodium chloride; potassium carbonate; sodium thiosulfate / tetrahydrofuran; tetrahydrofuran (10 ml)-methanol

With hydrogenchloride; sodium hydroxide; sodium chloride; sodium hydrogencarbonate; potassium carbonate; sodium thiosulfate; In tetrahydrofuran; tetrahydrofuran (10 ml)-methanol; N,N-dimethyl-formamide;

Reference yield:

: 626-55-1,163928-56-1
3-Bromopyridine

: 250601-34-4
E-2-[4-(5-methyl-2-phenyl-4-oxazolylmethoxy)benzyloxyimino]-2-(pyridine-1-oxide-3-yl)acetic acid

Guidance literature:: Multi-step reaction with 4 steps

1: hydrogenchloride; sodium chloride; sodium hydrogencarbonate / diethyl ether

2: sodium chloride; hydroxylamine hydrochloride; sodium acetate / ethanol; water

3: hydrogenchloride; sodium chloride; sodium hydrogencarbonate / N,N-dimethyl-formamide

4: hydrogenchloride; sodium hydroxide; sodium chloride; potassium carbonate; sodium thiosulfate / tetrahydrofuran; tetrahydrofuran (10 ml)-methanol

With hydrogenchloride; sodium hydroxide; sodium chloride; hydroxylamine hydrochloride; sodium acetate; sodium hydrogencarbonate; potassium carbonate; sodium thiosulfate; In tetrahydrofuran; tetrahydrofuran (10 ml)-methanol; diethyl ether; ethanol; water; N,N-dimethyl-formamide;