C₄₀H₄₄N₄O₄

Base Information

Chemical Name:C₄₀H₄₄N₄O₄
CAS No.:1383718-02-2
Molecular Formula:C₄₀H₄₄N₄O₄
Molecular Weight:644.814
Hs Code.:

C<sub>40</sub>H<sub>44</sub>N<sub>4</sub>O<sub>4</sub>

Synonyms:

Suppliers and Price of C₄₀H₄₄N₄O₄

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 C₄₀H₄₄N₄O₄

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₄₀H₄₄N₄O₄

There total 14 articles about C₄₀H₄₄N₄O₄ 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:

: 1383718-03-3
methyl 1-[2,4-bis(benzyloxy)cumenyl]-5-[p-(bromomethyl)-phenyl]-1H-1,2,3-triazole-4-carboxylate

: 108-91-8,157973-60-9
cyclohexylamine

: 1383718-02-2
C₄₀H₄₄N₄O₄

Guidance literature:: With triethylamine; In N,N-dimethyl-formamide; at 20 ℃;
DOI:10.1021/jm401536b

Reference yield:

: 100-39-0
benzyl bromide

: 1383718-02-2
C₄₀H₄₄N₄O₄

Guidance literature:: Multi-step reaction with 10 steps

1.1: potassium carbonate / acetonitrile

2.1: n-butyllithium / tetrahydrofuran

3.1: palladium on activated charcoal; hydrogen / ethanol / 20 °C / 760.05 Torr

3.2: 0.25 h / 20 °C

3.3: 3 h / Reflux

4.1: nitric acid; acetic acid / 0.5 h / 70 °C

5.1: tin(II) chloride dihdyrate; hydrogenchloride / ethanol / 3 h / 80 °C

6.1: tert.-butylnitrite; trimethylsilylazide / acetonitrile / 13 h / 0 - 20 °C

7.1: chloro(pentamethylcyclopentadienyl)ruthenium(II) tetramer / N,N-dimethyl-formamide / 12 h / 20 °C

8.1: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C

9.1: triphenylphosphine; carbon tetrabromide / dichloromethane

10.1: triethylamine / N,N-dimethyl-formamide / 20 °C

With hydrogenchloride; n-butyllithium; tert.-butylnitrite; tin(II) chloride dihdyrate; chloro(pentamethylcyclopentadienyl)ruthenium(II) tetramer; carbon tetrabromide; trimethylsilylazide; palladium on activated charcoal; tetrabutyl ammonium fluoride; hydrogen; nitric acid; potassium carbonate; acetic acid; triethylamine; triphenylphosphine; In tetrahydrofuran; ethanol; dichloromethane; N,N-dimethyl-formamide; acetonitrile; 7.1: |Huisgen Cycloaddition;
DOI:10.1021/jm401536b

Reference yield:

: 1383717-80-3
2,4-bis-(benzyloxy)-5-isopropylaniline

: 1383718-02-2
C₄₀H₄₄N₄O₄

Guidance literature:: Multi-step reaction with 5 steps

1: tert.-butylnitrite; trimethylsilylazide / acetonitrile / 13 h / 0 - 20 °C

2: chloro(pentamethylcyclopentadienyl)ruthenium(II) tetramer / N,N-dimethyl-formamide / 12 h / 20 °C

3: tetrabutyl ammonium fluoride / tetrahydrofuran / 2 h / 20 °C

4: triphenylphosphine; carbon tetrabromide / dichloromethane

5: triethylamine / N,N-dimethyl-formamide / 20 °C

With tert.-butylnitrite; chloro(pentamethylcyclopentadienyl)ruthenium(II) tetramer; carbon tetrabromide; trimethylsilylazide; tetrabutyl ammonium fluoride; triethylamine; triphenylphosphine; In tetrahydrofuran; dichloromethane; N,N-dimethyl-formamide; acetonitrile; 2: |Huisgen Cycloaddition;
DOI:10.1021/jm401536b