C₄₀H₃₈O₁₆

Base Information

Chemical Name:C₄₀H₃₈O₁₆
CAS No.:1362203-27-7
Molecular Formula:C₄₀H₃₈O₁₆
Molecular Weight:774.732
Hs Code.:

C<sub>40</sub>H<sub>38</sub>O<sub>16</sub>

Synonyms:

Suppliers and Price of C₄₀H₃₈O₁₆

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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 C₄₀H₃₈O₁₆

Chemical Property:

Purity/Quality:

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Technology Process of C₄₀H₃₈O₁₆

There total 6 articles about C₄₀H₃₈O₁₆ 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:

: 89385-62-6
C₅₅H₅₀O₈

: 1362203-27-7
C₄₀H₃₈O₁₆

Guidance literature:: Multi-step reaction with 2 steps

1: palladium on activated charcoal; hydrogen / tetrahydrofuran; methanol; dichloromethane / 24 h / 20 °C

2: iron(II) ammonium sulfate; recombinant N-terminally His6-tagged Vitis vinifera cabernet sauvignon leucoanthocyanidin dioxygenase; α-ketoglutaric acid; sodium L-ascorbate; bovine catalase / 1 h / 30 °C / pH 6 / aq. phosphate buffer; Enzymatic reaction

With iron(II) ammonium sulfate; α-ketoglutaric acid; palladium on activated charcoal; recombinant N-terminally His₆-tagged Vitis vinifera cabernet sauvignon leucoanthocyanidin dioxygenase; hydrogen; sodium L-ascorbate; bovine catalase; In tetrahydrofuran; methanol; dichloromethane;
DOI:10.1002/cbic.201100044

Reference yield:

: 154-23-4
catechin

: 1362203-27-7
C₄₀H₃₈O₁₆

Guidance literature:: Multi-step reaction with 6 steps

1: potassium carbonate / N,N-dimethyl-formamide / 48 h / 20 °C

2: sodium hydride / N,N-dimethyl-formamide / 6 h / 0 °C

3: trichlorophosphate / 19 h / 20 - 75 °C

4: sodium hydride / N,N-dimethyl-formamide / 15 h / 20 °C

5: palladium on activated charcoal; hydrogen / tetrahydrofuran; methanol; dichloromethane / 24 h / 20 °C

6: iron(II) ammonium sulfate; recombinant N-terminally His6-tagged Vitis vinifera cabernet sauvignon leucoanthocyanidin dioxygenase; α-ketoglutaric acid; sodium L-ascorbate; bovine catalase / 1 h / 30 °C / pH 6 / aq. phosphate buffer; Enzymatic reaction

With iron(II) ammonium sulfate; α-ketoglutaric acid; palladium on activated charcoal; recombinant N-terminally His₆-tagged Vitis vinifera cabernet sauvignon leucoanthocyanidin dioxygenase; hydrogen; sodium hydride; potassium carbonate; sodium L-ascorbate; bovine catalase; trichlorophosphate; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; 3: Vilsmeier-Haack reaction / 4: Horner-Wadsworth-Emmons olefination;
DOI:10.1002/cbic.201100044

Reference yield:

: 20728-73-8
5,7,3',4'-tetra-O-benzyl-(+)-catechin

: 1362203-27-7
C₄₀H₃₈O₁₆

Guidance literature:: Multi-step reaction with 5 steps

1: sodium hydride / N,N-dimethyl-formamide / 6 h / 0 °C

2: trichlorophosphate / 19 h / 20 - 75 °C

3: sodium hydride / N,N-dimethyl-formamide / 15 h / 20 °C

4: palladium on activated charcoal; hydrogen / tetrahydrofuran; methanol; dichloromethane / 24 h / 20 °C

5: iron(II) ammonium sulfate; recombinant N-terminally His6-tagged Vitis vinifera cabernet sauvignon leucoanthocyanidin dioxygenase; α-ketoglutaric acid; sodium L-ascorbate; bovine catalase / 1 h / 30 °C / pH 6 / aq. phosphate buffer; Enzymatic reaction

With iron(II) ammonium sulfate; α-ketoglutaric acid; palladium on activated charcoal; recombinant N-terminally His₆-tagged Vitis vinifera cabernet sauvignon leucoanthocyanidin dioxygenase; hydrogen; sodium hydride; sodium L-ascorbate; bovine catalase; trichlorophosphate; In tetrahydrofuran; methanol; dichloromethane; N,N-dimethyl-formamide; 2: Vilsmeier-Haack reaction / 3: Horner-Wadsworth-Emmons olefination;
DOI:10.1002/cbic.201100044