Butanoic acid, 4,4'-[[4-[[[5-[[[2-(4-ethoxy-4-oxobutoxy)-5-methylphenyl]amino]carbonyl]- 2,4-dimethoxyphenyl]amino]carbonyl]-6-nitro-1,3-phenylene]bis(oxy)]bis -, diethyl ester

Base Information

Chemical Name:Butanoic acid, 4,4'-[[4-[[[5-[[[2-(4-ethoxy-4-oxobutoxy)-5-methylphenyl]amino]carbonyl]- 2,4-dimethoxyphenyl]amino]carbonyl]-6-nitro-1,3-phenylene]bis(oxy)]bis -, diethyl ester
CAS No.:874210-71-6
Molecular Formula:C41H51N3O15
Molecular Weight:825.867
Hs Code.:

Butanoic acid,
4,4'-[[4-[[[5-[[[2-(4-ethoxy-4-oxobutoxy)-5-methylphenyl]amino]carbonyl]-
2,4-dimethoxyphenyl]amino]carbonyl]-6-nitro-1,3-phenylene]bis(oxy)]bis
-, diethyl ester

Synonyms:

Suppliers and Price of Butanoic acid, 4,4'-[[4-[[[5-[[[2-(4-ethoxy-4-oxobutoxy)-5-methylphenyl]amino]carbonyl]- 2,4-dimethoxyphenyl]amino]carbonyl]-6-nitro-1,3-phenylene]bis(oxy)]bis -, diethyl 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, 4,4'-[[4-[[[5-[[[2-(4-ethoxy-4-oxobutoxy)-5-methylphenyl]amino]carbonyl]- 2,4-dimethoxyphenyl]amino]carbonyl]-6-nitro-1,3-phenylene]bis(oxy)]bis -, diethyl ester

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of Butanoic acid, 4,4'-[[4-[[[5-[[[2-(4-ethoxy-4-oxobutoxy)-5-methylphenyl]amino]carbonyl]- 2,4-dimethoxyphenyl]amino]carbonyl]-6-nitro-1,3-phenylene]bis(oxy)]bis -, diethyl ester

There total 13 articles about Butanoic acid, 4,4'-[[4-[[[5-[[[2-(4-ethoxy-4-oxobutoxy)-5-methylphenyl]amino]carbonyl]- 2,4-dimethoxyphenyl]amino]carbonyl]-6-nitro-1,3-phenylene]bis(oxy)]bis -, diethyl 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: 73.3%

: 4-[2-(5-amino-2,4-dimethoxy-benzoylamino)-4-methyl-phenoxy]-butyric acid ethyl ester

: 874210-23-8
2,4-bis[3-(ethoxycarbonyl)propoxy]-5-nitrobenzoic acid

: 874210-71-6
4-(5-(3-ethoxycarbonyl-propoxy)-2-{5-[2-(3-ethoxycarbonyl-propoxy)-5-methyl-phenylcarbamoyl]-2,4-dimethoxy-phenylcarbamoyl}-4-nitro-phenoxy)-butyric acid ethyl ester

Guidance literature:: With chloro(triphenyl)phosphonium chloride; In dichloromethane; for 12h; Heating;
DOI:10.1021/jo050798a

Reference yield:

: 874210-51-2
4-(4-methyl-2-nitrophenoxy)butyric acid ethyl ester

: 874210-71-6
4-(5-(3-ethoxycarbonyl-propoxy)-2-{5-[2-(3-ethoxycarbonyl-propoxy)-5-methyl-phenylcarbamoyl]-2,4-dimethoxy-phenylcarbamoyl}-4-nitro-phenoxy)-butyric acid ethyl ester

Guidance literature:: Multi-step reaction with 4 steps

1: H₂ / Pd/C / ethanol / 2 h / 30 °C / 0.03 Torr

2: 0.48 g / Ph₃PCl₂ / CH₂Cl₂ / 4 h / Heating

3: 0.93 g / H₂ / Pd/C / CH₂Cl₂; dimethylformamide / 4 h / 50 °C / 0.03 Torr

4: 73.3 percent / Ph₃PCl₂ / CH₂Cl₂ / 12 h / Heating

With hydrogen; chloro(triphenyl)phosphonium chloride; palladium on activated charcoal; In ethanol; dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo050798a

Reference yield:

: 874210-70-5
4-[2-(2,4-dimethoxy-5-nitro-benzoylamino)-4-methyl-phenoxy]-butyric acid ethyl ester

: 874210-71-6
4-(5-(3-ethoxycarbonyl-propoxy)-2-{5-[2-(3-ethoxycarbonyl-propoxy)-5-methyl-phenylcarbamoyl]-2,4-dimethoxy-phenylcarbamoyl}-4-nitro-phenoxy)-butyric acid ethyl ester

Guidance literature:: Multi-step reaction with 2 steps

1: 0.93 g / H₂ / Pd/C / CH₂Cl₂; dimethylformamide / 4 h / 50 °C / 0.03 Torr

2: 73.3 percent / Ph₃PCl₂ / CH₂Cl₂ / 12 h / Heating

With hydrogen; chloro(triphenyl)phosphonium chloride; palladium on activated charcoal; In dichloromethane; N,N-dimethyl-formamide;
DOI:10.1021/jo050798a