C₃₁H₄₁N₅O₆

Base Information

Chemical Name:C₃₁H₄₁N₅O₆
CAS No.:1581709-50-3
Molecular Formula:C₃₁H₄₁N₅O₆
Molecular Weight:579.696
Hs Code.:

C<sub>31</sub>H<sub>41</sub>N<sub>5</sub>O<sub>6</sub>

Synonyms:C₃₁H₄₁N₅O₆

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Chemical Property of C₃₁H₄₁N₅O₆

Chemical Property:

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Technology Process of C₃₁H₄₁N₅O₆

There total 16 articles about C₃₁H₄₁N₅O₆ 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: 93.0%

: 1581709-49-0
C₄₅H₅₃N₅O₆

: 1581709-50-3
C₃₁H₄₁N₅O₆

Guidance literature:: With boron trichloride; In dichloromethane; at 20 ℃; for 3h;
DOI:10.1021/jm401536b

Reference yield:

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

: 1581709-50-3
C₃₁H₄₁N₅O₆

Guidance literature:: Multi-step reaction with 8 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

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

Reference yield:

: C₂₃H₂₁N₃O₂

: 1581709-50-3
C₃₁H₄₁N₅O₆

Guidance literature:: Multi-step reaction with 7 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

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