C₃₆H₃₈N₄O₄

Base Information

Chemical Name:C₃₆H₃₈N₄O₄
CAS No.:494857-52-2
Molecular Formula:C₃₆H₃₈N₄O₄
Molecular Weight:590.722
Hs Code.:

C<sub>36</sub>H<sub>38</sub>N<sub>4</sub>O<sub>4</sub>

Synonyms:C₃₆H₃₈N₄O₄

Suppliers and Price of C₃₆H₃₈N₄O₄

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 C₃₆H₃₈N₄O₄

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₃₆H₃₈N₄O₄

There total 14 articles about C₃₆H₃₈N₄O₄ 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:

: 22264-50-2
1-aminocyclobutane-1-carboxylic acid

: 494857-52-2
C₃₆H₃₈N₄O₄

Guidance literature:: Multi-step reaction with 3 steps

1: potassium phosphate / acetonitrile / 20 °C / Inert atmosphere

2: dimethyl sulfoxide / 20 °C / Inert atmosphere

3: water / 20 °C / Alkaline conditions; Inert atmosphere

With potassium phosphate; water; In dimethyl sulfoxide; acetonitrile;
DOI:10.1021/jm3006788

Reference yield:

: 1670-82-2,261352-47-0
Indole-6-carboxylic acid

: 494857-52-2
C₃₆H₃₈N₄O₄

Guidance literature:: Multi-step reaction with 9 steps

1.1: potassium hydroxide / methanol; water / 21 h / 75 °C / Inert atmosphere

2.1: 20% Pd(OH)2/C; hydrogen / methanol / 18 h / 760.05 Torr / Inert atmosphere

3.1: potassium carbonate / N,N-dimethyl-formamide / 5 h / 20 °C / Inert atmosphere

3.2: 0 - 20 °C / Inert atmosphere

4.1: bromine; sodium acetate / Isopropyl acetate / 4 - 13 °C / Inert atmosphere

5.1: n-butyllithium / tetrahydrofuran; hexane / -72 - -68 °C / Inert atmosphere

5.2: -72 - 20 °C / Inert atmosphere

6.1: copper(l) iodide; triphenylphosphine; lithium chloride / N,N-dimethyl-formamide / 0.75 h / Inert atmosphere

6.2: 2 h / 100 °C / Inert atmosphere

7.1: water; sodium hydroxide / tetrahydrofuran; methanol / 60 °C / Inert atmosphere

8.1: dimethyl sulfoxide / 20 °C / Inert atmosphere

9.1: water / 20 °C / Alkaline conditions; Inert atmosphere

With copper(l) iodide; n-butyllithium; 20% Pd(OH)2/C; water; hydrogen; bromine; sodium acetate; potassium carbonate; triphenylphosphine; lithium chloride; potassium hydroxide; sodium hydroxide; In tetrahydrofuran; methanol; hexane; Isopropyl acetate; water; dimethyl sulfoxide; N,N-dimethyl-formamide; 6.1: |Stille Cross Coupling / 6.2: |Stille Cross Coupling;
DOI:10.1021/jm3006788

Reference yield:

: 120-92-3
cyclopentanone

: 494857-52-2
C₃₆H₃₈N₄O₄

Guidance literature:: Multi-step reaction with 9 steps

1.1: potassium hydroxide / methanol; water / 21 h / 75 °C / Inert atmosphere

2.1: 20% Pd(OH)2/C; hydrogen / methanol / 18 h / 760.05 Torr / Inert atmosphere

3.1: potassium carbonate / N,N-dimethyl-formamide / 5 h / 20 °C / Inert atmosphere

3.2: 0 - 20 °C / Inert atmosphere

4.1: bromine; sodium acetate / Isopropyl acetate / 4 - 13 °C / Inert atmosphere

5.1: n-butyllithium / tetrahydrofuran; hexane / -72 - -68 °C / Inert atmosphere

5.2: -72 - 20 °C / Inert atmosphere

6.1: copper(l) iodide; triphenylphosphine; lithium chloride / N,N-dimethyl-formamide / 0.75 h / Inert atmosphere

6.2: 2 h / 100 °C / Inert atmosphere

7.1: water; sodium hydroxide / tetrahydrofuran; methanol / 60 °C / Inert atmosphere

8.1: dimethyl sulfoxide / 20 °C / Inert atmosphere

9.1: water / 20 °C / Alkaline conditions; Inert atmosphere

With copper(l) iodide; n-butyllithium; 20% Pd(OH)2/C; water; hydrogen; bromine; sodium acetate; potassium carbonate; triphenylphosphine; lithium chloride; potassium hydroxide; sodium hydroxide; In tetrahydrofuran; methanol; hexane; Isopropyl acetate; water; dimethyl sulfoxide; N,N-dimethyl-formamide; 6.1: |Stille Cross Coupling / 6.2: |Stille Cross Coupling;
DOI:10.1021/jm3006788