C₂₉H₄₂O₅S₂Sn

Base Information

Chemical Name:C₂₉H₄₂O₅S₂Sn
CAS No.:861108-20-5
Molecular Formula:C₂₉H₄₂O₅S₂Sn
Molecular Weight:653.491
Hs Code.:

C<sub>29</sub>H<sub>42</sub>O<sub>5</sub>S<sub>2</sub>Sn

Synonyms:

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Chemical Property of C₂₉H₄₂O₅S₂Sn

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Technology Process of C₂₉H₄₂O₅S₂Sn

There total 6 articles about C₂₉H₄₂O₅S₂Sn 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:

: 5656-44-0
4-(allylthio)phenol

: 861108-20-5
C₂₉H₄₂O₅S₂Sn

Guidance literature:: Multi-step reaction with 4 steps

1: N,N-dimethylglycine hydrochoride; caesium carbonate / copper(l) iodide / 1,4-dioxane / 22 h / 90 °C

2: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 192 h / 0 - 20 °C

3: thiourea / methanol; dichloromethane / 20 °C

4: toluene / 12 h / 80 °C

With N,N-dimethylglycine hydrochoride; caesium carbonate; thiourea; 3-chloro-benzenecarboperoxoic acid; copper(l) iodide; In 1,4-dioxane; methanol; dichloromethane; toluene; 1: Ullmann Coupling / 4: Mascaretti;

Reference yield:

: 41841-16-1
(4-bromo-phenyl)-acetic acid methyl ester

: 861108-20-5
C₂₉H₄₂O₅S₂Sn

Guidance literature:: Multi-step reaction with 4 steps

1: N,N-dimethylglycine hydrochoride; caesium carbonate / copper(l) iodide / 1,4-dioxane / 22 h / 90 °C

2: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 192 h / 0 - 20 °C

3: thiourea / methanol; dichloromethane / 20 °C

4: toluene / 12 h / 80 °C

With N,N-dimethylglycine hydrochoride; caesium carbonate; thiourea; 3-chloro-benzenecarboperoxoic acid; copper(l) iodide; In 1,4-dioxane; methanol; dichloromethane; toluene; 1: Ullmann Coupling / 4: Mascaretti;

Reference yield:

: 637-89-8
4-sulfanylphenol

: 861108-20-5
C₂₉H₄₂O₅S₂Sn

Guidance literature:: Multi-step reaction with 5 steps

1: potassium carbonate / N,N-dimethyl-formamide / 0 - 20 °C

2: N,N-dimethylglycine hydrochoride; caesium carbonate / copper(l) iodide / 1,4-dioxane / 22 h / 90 °C

3: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 192 h / 0 - 20 °C

4: thiourea / methanol; dichloromethane / 20 °C

5: toluene / 12 h / 80 °C

With N,N-dimethylglycine hydrochoride; potassium carbonate; caesium carbonate; thiourea; 3-chloro-benzenecarboperoxoic acid; copper(l) iodide; In 1,4-dioxane; methanol; dichloromethane; N,N-dimethyl-formamide; toluene; 2: Ullmann Coupling / 5: Mascaretti;