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C25H28O2

Base Information Edit
C<sub>25</sub>H<sub>28</sub>O<sub>2</sub>

Synonyms:C25H28O2

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of C25H28O2 Edit
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Technology Process of C25H28O2

There total 7 articles about C25H28O2 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:
Guidance literature:
With hydrogenchloride; water; at 20 ℃; for 0.5h; pH=4 - 6;
DOI:10.1016/j.ejmech.2013.01.012
Guidance literature:
Multi-step reaction with 6 steps
1.1: palladium 10% on activated carbon; hydrogen / methanol / 24 h / 7600.51 Torr
2.1: polyphosphoric acid / 12 h / 80 °C
3.1: lithium diisopropyl amide / tetrahydrofuran / 0.5 h / -78 °C
3.2: 4 h / -78 °C
4.1: acetic acid; sulfuric acid / 4 h / 20 °C
5.1: sodium methylate / methanol / 0.5 h / 20 °C
5.2: 4 h / 80 °C
6.1: hydrogenchloride; water / 0.5 h / 20 °C / pH 4 - 6
With hydrogenchloride; sulfuric acid; palladium 10% on activated carbon; water; hydrogen; sodium methylate; acetic acid; lithium diisopropyl amide; In tetrahydrofuran; methanol; 2.1: |Friedel-Crafts Acylation / 5.1: |Claisen-Schmidt Condensation / 5.2: |Claisen-Schmidt Condensation;
DOI:10.1016/j.ejmech.2013.01.012
Guidance literature:
Multi-step reaction with 5 steps
1.1: polyphosphoric acid / 12 h / 80 °C
2.1: lithium diisopropyl amide / tetrahydrofuran / 0.5 h / -78 °C
2.2: 4 h / -78 °C
3.1: acetic acid; sulfuric acid / 4 h / 20 °C
4.1: sodium methylate / methanol / 0.5 h / 20 °C
4.2: 4 h / 80 °C
5.1: hydrogenchloride; water / 0.5 h / 20 °C / pH 4 - 6
With hydrogenchloride; sulfuric acid; water; sodium methylate; acetic acid; lithium diisopropyl amide; In tetrahydrofuran; methanol; 1.1: |Friedel-Crafts Acylation / 4.1: |Claisen-Schmidt Condensation / 4.2: |Claisen-Schmidt Condensation;
DOI:10.1016/j.ejmech.2013.01.012
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