C₃₆H₄₂N₄O₅

Base Information

Chemical Name:C₃₆H₄₂N₄O₅
CAS No.:1613625-34-5
Molecular Formula:C₃₆H₄₂N₄O₅
Molecular Weight:610.753
Hs Code.:

C<sub>36</sub>H<sub>42</sub>N<sub>4</sub>O<sub>5</sub>

Synonyms:C₃₆H₄₂N₄O₅

Suppliers and Price of C₃₆H₄₂N₄O₅

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 C₃₆H₄₂N₄O₅

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₃₆H₄₂N₄O₅

There total 21 articles about C₃₆H₄₂N₄O₅ 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:

: 1613625-33-4
C₄₁H₅₀N₄O₇

: 1613625-34-5
C₃₆H₄₂N₄O₅

Guidance literature:: With hydrogenchloride; In 1,4-dioxane; at 20 ℃; for 1h;

Reference yield:

: 15971-29-6
4-methoxy-1-naphthaldehyde

: 1613625-34-5
C₃₆H₄₂N₄O₅

Guidance literature:: Multi-step reaction with 21 steps

1.1: 1,8-diazabicyclo[5.4.0]undec-7-ene / dichloromethane / 0.25 h / 0 °C

1.2: 36 h / 20 °C

2.1: hydrogen; palladium 10% on activated carbon / ethanol / 16 h / 20 °C / 760.05 Torr

3.1: sodium hydroxide; water / tetrahydrofuran; methanol / 1 h / 20 °C

4.1: n-butyllithium / tetrahydrofuran; cyclohexane / 1 h / -78 °C

4.2: 1.8 h / -78 - 20 °C

5.1: potassium hexamethylsilazane / tetrahydrofuran / 0.5 h / -78 °C

5.2: 0.08 h / -78 °C

5.3: 16 h / -78 - 24 °C

6.1: dihydrogen peroxide; lithium hydroxide / tetrahydrofuran; water / 1.2 h / 0 - 20 °C

7.1: hydrogen; palladium 10% on activated carbon / water / 3 h / 20 °C / 760.05 Torr

8.1: acetic acid; hydrogen bromide / 3 h / Reflux

9.1: acetyl chloride / 4 h / 0 °C / Reflux

10.1: sodium hydrogencarbonate / methanol; water / 1 h / 0 - 20 °C

11.1: pyridine / 2 h / 0 - 20 °C

12.1: tri-tert-butyl phosphine; copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; triethylamine / acetonitrile; hexane / 16 h / Inert atmosphere; Reflux

13.1: sodium hydroxide; water / tetrahydrofuran; methanol / 2 h / 20 °C

14.1: 4-methyl-morpholine; pivaloyl chloride / tetrahydrofuran / 2 h / 0 °C

15.1: ammonia / methanol / 18 h / 0 - 20 °C

16.1: hydrogen; palladium 10% on activated carbon / ethanol / 16 h / 20 °C / 760.05 Torr

17.1: sodium hydrogencarbonate / methanol; water / 0.17 h / 0 °C

17.2: 2 h / 0 - 20 °C

18.1: hydrogenchloride / 1,4-dioxane / 1 h / 20 °C

19.1: acetic acid; sodium cyanoborohydride / 2.7 h / 20 °C

20.1: sodium hydrogencarbonate / methanol; water / 0.17 h / 0 °C

20.2: 2 h / 0 - 20 °C

21.1: hydrogenchloride / 1,4-dioxane / 1 h / 20 °C

With 4-methyl-morpholine; pyridine; hydrogenchloride; copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; n-butyllithium; tri-tert-butyl phosphine; palladium 10% on activated carbon; ammonia; water; hydrogen bromide; hydrogen; dihydrogen peroxide; pivaloyl chloride; potassium hexamethylsilazane; sodium cyanoborohydride; sodium hydrogencarbonate; acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; acetyl chloride; sodium hydroxide; lithium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; hexane; dichloromethane; cyclohexane; water; acetonitrile;

Reference yield:

: methyl-3-(4-methoxy-1-naphthyl)-E-propenoate

: 1613625-34-5
C₃₆H₄₂N₄O₅

Guidance literature:: Multi-step reaction with 20 steps

1.1: hydrogen; palladium 10% on activated carbon / ethanol / 16 h / 20 °C / 760.05 Torr

2.1: sodium hydroxide; water / tetrahydrofuran; methanol / 1 h / 20 °C

3.1: n-butyllithium / tetrahydrofuran; cyclohexane / 1 h / -78 °C

3.2: 1.8 h / -78 - 20 °C

4.1: potassium hexamethylsilazane / tetrahydrofuran / 0.5 h / -78 °C

4.2: 0.08 h / -78 °C

4.3: 16 h / -78 - 24 °C

5.1: dihydrogen peroxide; lithium hydroxide / tetrahydrofuran; water / 1.2 h / 0 - 20 °C

6.1: hydrogen; palladium 10% on activated carbon / water / 3 h / 20 °C / 760.05 Torr

7.1: acetic acid; hydrogen bromide / 3 h / Reflux

8.1: acetyl chloride / 4 h / 0 °C / Reflux

9.1: sodium hydrogencarbonate / methanol; water / 1 h / 0 - 20 °C

10.1: pyridine / 2 h / 0 - 20 °C

11.1: tri-tert-butyl phosphine; copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; triethylamine / acetonitrile; hexane / 16 h / Inert atmosphere; Reflux

12.1: sodium hydroxide; water / tetrahydrofuran; methanol / 2 h / 20 °C

13.1: 4-methyl-morpholine; pivaloyl chloride / tetrahydrofuran / 2 h / 0 °C

14.1: ammonia / methanol / 18 h / 0 - 20 °C

15.1: hydrogen; palladium 10% on activated carbon / ethanol / 16 h / 20 °C / 760.05 Torr

16.1: sodium hydrogencarbonate / methanol; water / 0.17 h / 0 °C

16.2: 2 h / 0 - 20 °C

17.1: hydrogenchloride / 1,4-dioxane / 1 h / 20 °C

18.1: acetic acid; sodium cyanoborohydride / 2.7 h / 20 °C

19.1: sodium hydrogencarbonate / methanol; water / 0.17 h / 0 °C

19.2: 2 h / 0 - 20 °C

20.1: hydrogenchloride / 1,4-dioxane / 1 h / 20 °C

With 4-methyl-morpholine; pyridine; hydrogenchloride; copper(l) iodide; tetrakis(triphenylphosphine) palladium⁽⁰⁾; n-butyllithium; tri-tert-butyl phosphine; palladium 10% on activated carbon; ammonia; water; hydrogen bromide; hydrogen; dihydrogen peroxide; pivaloyl chloride; potassium hexamethylsilazane; sodium cyanoborohydride; sodium hydrogencarbonate; acetic acid; triethylamine; acetyl chloride; sodium hydroxide; lithium hydroxide; In tetrahydrofuran; 1,4-dioxane; methanol; ethanol; hexane; cyclohexane; water; acetonitrile;