C₂₈H₃₄N₁₂O₆

Base Information

Chemical Name:C₂₈H₃₄N₁₂O₆
CAS No.:755017-84-6
Molecular Formula:C₂₈H₃₄N₁₂O₆
Molecular Weight:634.655
Hs Code.:

C<sub>28</sub>H<sub>34</sub>N<sub>12</sub>O<sub>6</sub>

Synonyms:C₂₈H₃₄N₁₂O₆

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Chemical Property of C₂₈H₃₄N₁₂O₆

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Technology Process of C₂₈H₃₄N₁₂O₆

There total 6 articles about C₂₈H₃₄N₁₂O₆ 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:

: 6337-67-3
4,4'-bis(bromomethyl)bibenzyl

: 755017-84-6
C₂₈H₃₄N₁₂O₆

Guidance literature:: Multi-step reaction with 2 steps

1: 96 percent / NaH; TBAI / dimethylformamide / 2 h / 20 °C

2: aq. acetic acid / dioxane / 10 h / 75 - 80 °C

With tetra-(n-butyl)ammonium iodide; sodium hydride; acetic acid; In 1,4-dioxane; N,N-dimethyl-formamide;
DOI:10.1021/ja048936l

Reference yield:

: 236115-61-0
[(1S,2S,3R,4S,6R)-2-acetoxy-4,6-diazido-3-hydroxy-cyclohexyl] acetate

: 755017-84-6
C₂₈H₃₄N₁₂O₆

Guidance literature:: Multi-step reaction with 6 steps

1: 92 percent / imidazole / dimethylformamide / 24 h / 20 °C

2: 93 percent / sodium methoxide / methanol / 5 h / 20 °C

3: 95 percent / p-toluenesulfonic acid / 10 h / 20 °C

4: 100 percent / tetrabutylammonium fluoride / tetrahydrofuran / 1 h / 20 °C

5: 96 percent / NaH; TBAI / dimethylformamide / 2 h / 20 °C

6: aq. acetic acid / dioxane / 10 h / 75 - 80 °C

With 1H-imidazole; tetrabutyl ammonium fluoride; sodium methylate; tetra-(n-butyl)ammonium iodide; sodium hydride; toluene-4-sulfonic acid; acetic acid; In tetrahydrofuran; 1,4-dioxane; methanol; N,N-dimethyl-formamide;
DOI:10.1021/ja048936l

Reference yield:

: 844665-82-3
2-deoxy-1,3-diazido-4-O-t-butyldimethylsilyl-5,6-di-O-acetylstreptamine

: 755017-84-6
C₂₈H₃₄N₁₂O₆

Guidance literature:: Multi-step reaction with 5 steps

1: 93 percent / sodium methoxide / methanol / 5 h / 20 °C

2: 95 percent / p-toluenesulfonic acid / 10 h / 20 °C

3: 100 percent / tetrabutylammonium fluoride / tetrahydrofuran / 1 h / 20 °C

4: 96 percent / NaH; TBAI / dimethylformamide / 2 h / 20 °C

5: aq. acetic acid / dioxane / 10 h / 75 - 80 °C

With tetrabutyl ammonium fluoride; sodium methylate; tetra-(n-butyl)ammonium iodide; sodium hydride; toluene-4-sulfonic acid; acetic acid; In tetrahydrofuran; 1,4-dioxane; methanol; N,N-dimethyl-formamide;
DOI:10.1021/ja048936l