C₃₀H₄₀N₆O₆

Base Information

Chemical Name:C₃₀H₄₀N₆O₆
CAS No.:1581709-47-8
Molecular Formula:C₃₀H₄₀N₆O₆
Molecular Weight:580.684
Hs Code.:

C<sub>30</sub>H<sub>40</sub>N<sub>6</sub>O<sub>6</sub>

Synonyms:C₃₀H₄₀N₆O₆

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Chemical Property of C₃₀H₄₀N₆O₆

Chemical Property:

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Technology Process of C₃₀H₄₀N₆O₆

There total 17 articles about C₃₀H₄₀N₆O₆ 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: 49.0%

: 1581709-50-3
C₃₁H₄₁N₅O₆

: 1581709-47-8
C₃₀H₄₀N₆O₆

Guidance literature:: With hydroxylamine; sodium hydroxide; In methanol; water; at 0 - 20 ℃; for 2h;
DOI:10.1021/jm401536b

Reference yield:

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

: 1581709-47-8
C₃₀H₄₀N₆O₆

Guidance literature:: Multi-step reaction with 9 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: triethylamine / dichloromethane / 12.5 h / 0 - 20 °C

5: triethylamine / N,N-dimethyl-formamide / 12 h / 20 °C

6: lithium hydroxide; water / tetrahydrofuran / 12 h / 20 °C

7: hydrogenchloride; N-ethyl-N,N-diisopropylamine; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate / dichloromethane / 6 h / 20 °C

8: boron trichloride / dichloromethane / 3 h / 20 °C

9: hydroxylamine; sodium hydroxide / methanol; water / 2 h / 0 - 20 °C

With hydrogenchloride; tert.-butylnitrite; chloro(pentamethylcyclopentadienyl)ruthenium(II) tetramer; trimethylsilylazide; tetrabutyl ammonium fluoride; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; water; hydroxylamine; boron trichloride; triethylamine; N-ethyl-N,N-diisopropylamine; sodium hydroxide; lithium hydroxide; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; acetonitrile; 2: |Huisgen Cycloaddition;
DOI:10.1021/jm401536b

Reference yield:

: C₂₃H₂₁N₃O₂

: 1581709-47-8
C₃₀H₄₀N₆O₆

Guidance literature:: Multi-step reaction with 8 steps

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

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

3: triethylamine / dichloromethane / 12.5 h / 0 - 20 °C

4: triethylamine / N,N-dimethyl-formamide / 12 h / 20 °C

5: lithium hydroxide; water / tetrahydrofuran / 12 h / 20 °C

6: hydrogenchloride; N-ethyl-N,N-diisopropylamine; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate / dichloromethane / 6 h / 20 °C

7: boron trichloride / dichloromethane / 3 h / 20 °C

8: hydroxylamine; sodium hydroxide / methanol; water / 2 h / 0 - 20 °C

With hydrogenchloride; chloro(pentamethylcyclopentadienyl)ruthenium(II) tetramer; tetrabutyl ammonium fluoride; benzotriazol-1-yloxyl-tris-(pyrrolidino)-phosphonium hexafluorophosphate; water; hydroxylamine; boron trichloride; triethylamine; N-ethyl-N,N-diisopropylamine; sodium hydroxide; lithium hydroxide; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; 1: |Huisgen Cycloaddition;
DOI:10.1021/jm401536b