C₃₀H₃₇N₃O₅

Base Information

Chemical Name:C₃₀H₃₇N₃O₅
CAS No.:1613625-30-1
Molecular Formula:C₃₀H₃₇N₃O₅
Molecular Weight:519.641
Hs Code.:

C<sub>30</sub>H<sub>37</sub>N<sub>3</sub>O<sub>5</sub>

Synonyms:C₃₀H₃₇N₃O₅

Suppliers and Price of C₃₀H₃₇N₃O₅

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 C₃₀H₃₇N₃O₅

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of C₃₀H₃₇N₃O₅

There total 17 articles about C₃₀H₃₇N₃O₅ 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: 89.0%

: C₂₂H₃₁N₃O₃*C₂H₄O₂

: 501-53-1,94274-21-2
benzyl chloroformate

: 1613625-30-1
C₃₀H₃₇N₃O₅

Guidance literature:: C₂₂H₃₁N₃O₃*C₂H₄O₂; With sodium hydrogencarbonate; In methanol; water; at 0 ℃; for 0.166667h;

benzyl chloroformate; In methanol; water; at 0 - 20 ℃; for 2h;

Reference yield:

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

: 1613625-30-1
C₃₀H₃₇N₃O₅

Guidance literature:: Multi-step reaction with 17 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

With 4-methyl-morpholine; pyridine; 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 hydrogencarbonate; acetic acid; 1,8-diazabicyclo[5.4.0]undec-7-ene; triethylamine; acetyl chloride; sodium hydroxide; lithium hydroxide; In tetrahydrofuran; methanol; ethanol; hexane; dichloromethane; cyclohexane; water; acetonitrile;

Reference yield:

: 33189-02-5
β-(4-methoxy-1-naphthyl)propionic acid

: 1613625-30-1
C₃₀H₃₇N₃O₅

Guidance literature:: Multi-step reaction with 14 steps

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

1.2: 1.8 h / -78 - 20 °C

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

2.2: 0.08 h / -78 °C

2.3: 16 h / -78 - 24 °C

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

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

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

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

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

8.1: pyridine / 2 h / 0 - 20 °C

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

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

11.1: 4-methyl-morpholine; pivaloyl chloride / tetrahydrofuran / 2 h / 0 °C

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

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

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

14.2: 2 h / 0 - 20 °C

With 4-methyl-morpholine; pyridine; 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 hydrogencarbonate; acetic acid; triethylamine; acetyl chloride; sodium hydroxide; lithium hydroxide; In tetrahydrofuran; methanol; ethanol; hexane; cyclohexane; water; acetonitrile;