C₂₆H₂₉Cl₂N₃O₆

Base Information

Chemical Name:C₂₆H₂₉Cl₂N₃O₆
CAS No.:1424337-10-9
Molecular Formula:C₂₆H₂₉Cl₂N₃O₆
Molecular Weight:550.439
Hs Code.:

C<sub>26</sub>H<sub>29</sub>Cl<sub>2</sub>N<sub>3</sub>O<sub>6</sub>

Synonyms:C₂₆H₂₉Cl₂N₃O₆

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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 C₂₆H₂₉Cl₂N₃O₆

Chemical Property:

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Technology Process of C₂₆H₂₉Cl₂N₃O₆

There total 13 articles about C₂₆H₂₉Cl₂N₃O₆ 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:

: C₂₉H₃₃Cl₂N₃O₆

: 1424337-10-9
C₂₆H₂₉Cl₂N₃O₆

Guidance literature:: With hydrogenchloride; In ethanol; water; at 20 ℃; for 12h;
DOI:10.1016/j.bmcl.2012.11.058

Reference yield:

: 1424337-17-6
3-(4-(1,3-dioxoisoindolin-2-yl)butoxy)-4-methoxybenzaldehyde

: 1424337-10-9
C₂₆H₂₉Cl₂N₃O₆

Guidance literature:: Multi-step reaction with 7 steps

1.1: sodium dihydrogenphosphate; sodium chlorite; dihydrogen peroxide / acetonitrile; water / 24.5 h / 15 - 20 °C

2.1: thionyl chloride / 6 h / Reflux

3.1: sodium hydride / tetrahydrofuran; mineral oil / 0.25 h / 20 °C

3.2: 1.5 h / 10 - 20 °C

4.1: hydrazine hydrate / ethanol / 2 h / Reflux

5.1: triethylamine / N,N-dimethyl-formamide / 24 h / 65 °C

6.1: ammonium fluoride / water; ethanol / 48 h / 45 °C

7.1: hydrogenchloride / water; ethanol / 12 h / 20 °C

With hydrogenchloride; ammonium fluoride; sodium chlorite; sodium dihydrogenphosphate; thionyl chloride; dihydrogen peroxide; sodium hydride; hydrazine hydrate; triethylamine; In tetrahydrofuran; ethanol; water; N,N-dimethyl-formamide; acetonitrile; mineral oil;
DOI:10.1016/j.bmcl.2012.11.058

Reference yield:

: 90-02-8
salicylaldehyde

: 1424337-10-9
C₂₆H₂₉Cl₂N₃O₆

Guidance literature:: Multi-step reaction with 8 steps

1: aluminum (III) chloride / dichloromethane / 15 h / Reflux

2: sodium tetrahydroborate; acetic acid / 1 h / 10 °C

3: dichloromethane / 10 h / 20 °C

4: sodium tetrahydroborate / methanol / 1 h / 0 - 20 °C

5: 1H-imidazole / N,N-dimethyl-formamide / 16 h / 20 °C

6: triethylamine / N,N-dimethyl-formamide / 24 h / 65 °C

7: ammonium fluoride / water; ethanol / 48 h / 45 °C

8: hydrogenchloride / water; ethanol / 12 h / 20 °C

With 1H-imidazole; hydrogenchloride; aluminum (III) chloride; ammonium fluoride; sodium tetrahydroborate; acetic acid; triethylamine; In methanol; ethanol; dichloromethane; water; N,N-dimethyl-formamide;
DOI:10.1016/j.bmcl.2012.11.058