C₂₉H₂₆N₂O₇S

Base Information

Chemical Name:C₂₉H₂₆N₂O₇S
CAS No.:1297474-49-7
Molecular Formula:C₂₉H₂₆N₂O₇S
Molecular Weight:546.601
Hs Code.:

C<sub>29</sub>H<sub>26</sub>N<sub>2</sub>O<sub>7</sub>S

Synonyms:

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Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

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Chemical Property of C₂₉H₂₆N₂O₇S

Chemical Property:

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Technology Process of C₂₉H₂₆N₂O₇S

There total 5 articles about C₂₉H₂₆N₂O₇S 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:

: 1297474-29-3
4-(3,5-dimethoxyphenyl)cyclohexan-1-one

: 1297474-49-7
C₂₉H₂₆N₂O₇S

Guidance literature:: Multi-step reaction with 3 steps

1: piperidine; sulfur / ethanol / 4 h / 50 °C

2: chloranil / 1,4-dioxane / 5 h / 90 °C

3: hydrogenchloride / butan-1-ol / 2 h / Reflux

With piperidine; hydrogenchloride; chloranil; sulfur; In 1,4-dioxane; ethanol; butan-1-ol; 1: Gewald reaction;
DOI:10.1016/j.tetlet.2010.12.081

Reference yield:

: 1297474-25-9
C₁₄H₁₆O₃

: 1297474-49-7
C₂₉H₂₆N₂O₇S

Guidance literature:: Multi-step reaction with 4 steps

1: palladium 10% on activated carbon; hydrogen / ethyl acetate / 16 h / 20 °C

2: piperidine; sulfur / ethanol / 4 h / 50 °C

3: chloranil / 1,4-dioxane / 5 h / 90 °C

4: hydrogenchloride / butan-1-ol / 2 h / Reflux

With piperidine; hydrogenchloride; palladium 10% on activated carbon; hydrogen; chloranil; sulfur; In 1,4-dioxane; ethanol; ethyl acetate; butan-1-ol; 2: Gewald reaction;
DOI:10.1016/j.tetlet.2010.12.081

Reference yield:

: 1297474-23-7
C₁₆H₂₂O₅

: 1297474-49-7
C₂₉H₂₆N₂O₇S

Guidance literature:: Multi-step reaction with 5 steps

1: trifluoroacetic acid / dichloromethane / 5 h / 20 °C

2: palladium 10% on activated carbon; hydrogen / ethyl acetate / 16 h / 20 °C

3: piperidine; sulfur / ethanol / 4 h / 50 °C

4: chloranil / 1,4-dioxane / 5 h / 90 °C

5: hydrogenchloride / butan-1-ol / 2 h / Reflux

With piperidine; hydrogenchloride; palladium 10% on activated carbon; hydrogen; chloranil; sulfur; trifluoroacetic acid; In 1,4-dioxane; ethanol; dichloromethane; ethyl acetate; butan-1-ol; 3: Gewald reaction;
DOI:10.1016/j.tetlet.2010.12.081