C₂₄H₄₀O₄S

Base Information

Chemical Name:C₂₄H₄₀O₄S
CAS No.:1648931-34-3
Molecular Formula:C₂₄H₄₀O₄S
Molecular Weight:424.645
Hs Code.:

C<sub>24</sub>H<sub>40</sub>O<sub>4</sub>S

Synonyms:C₂₄H₄₀O₄S

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Chemical Property of C₂₄H₄₀O₄S

Chemical Property:

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Technology Process of C₂₄H₄₀O₄S

There total 2 articles about C₂₄H₄₀O₄S 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:

: 1643949-37-4
C₂₅H₄₇NO₃S

: 1648931-34-3
C₂₄H₄₀O₄S

Guidance literature:: Multi-step reaction with 2 steps

1: lithium triethylborohydride / tetrahydrofuran / 0 °C / Inert atmosphere

2: triethylamine; dmap / dichloromethane / 2 h / 0 °C / Inert atmosphere

With dmap; lithium triethylborohydride; triethylamine; In tetrahydrofuran; dichloromethane;
DOI:10.1002/ejoc.201402221

Reference yield:

: 2765-11-9
n-pentadecanal

: 1648931-34-3
C₂₄H₄₀O₄S

Guidance literature:: Multi-step reaction with 3 steps

1: sodium hydroxide / tert-butyl alcohol / Inert atmosphere

2: lithium triethylborohydride / tetrahydrofuran / 0 °C / Inert atmosphere

3: triethylamine; dmap / dichloromethane / 2 h / 0 °C / Inert atmosphere

With dmap; lithium triethylborohydride; triethylamine; sodium hydroxide; In tetrahydrofuran; dichloromethane; tert-butyl alcohol;
DOI:10.1002/ejoc.201402221

Reference yield:

: 1648931-34-3
C₂₄H₄₀O₄S

: 554-62-1
D-ribo-phytosphingosine

Guidance literature:: Multi-step reaction with 7 steps

1.1: potassium iodide / N,N-dimethyl-formamide; acetone / 1.5 h / Inert atmosphere; Reflux

1.2: 1 h / 0 °C / Inert atmosphere

2.1: 1H-imidazole / N,N-dimethyl-formamide / 6 h / 25 °C / Inert atmosphere

3.1: osmium(VIII) oxide; 4-methylmorpholine N-oxide; tert-butyl alcohol / tetrahydrofuran / 25 °C / Inert atmosphere

4.1: sodium periodate; water / methanol / 2 h / 0 °C / Inert atmosphere

5.1: water; sodium hydroxide / dichloromethane / 25 °C / Inert atmosphere

6.1: sodium azide; acetic acid / N,N-dimethyl-formamide / 12 h / 70 °C / Inert atmosphere

7.1: lithium aluminium tetrahydride / tetrahydrofuran / 0 - 65 °C / Inert atmosphere

7.2: 0 °C / Inert atmosphere

With 1H-imidazole; sodium periodate; osmium(VIII) oxide; lithium aluminium tetrahydride; sodium azide; water; acetic acid; 4-methylmorpholine N-oxide; potassium iodide; sodium hydroxide; tert-butyl alcohol; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; acetone; 3.1: |Upjohn Dihydroxylation;
DOI:10.1002/ejoc.201402221