C₅₀H₆₆N₄O₈

Base Information

Chemical Name:C₅₀H₆₆N₄O₈
CAS No.:98977-24-3
Molecular Formula:C₅₀H₆₆N₄O₈
Molecular Weight:851.096
Hs Code.:

C<sub>50</sub>H<sub>66</sub>N<sub>4</sub>O<sub>8</sub>

Synonyms:C₅₀H₆₆N₄O₈

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Chemical Property of C₅₀H₆₆N₄O₈

Chemical Property:

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Technology Process of C₅₀H₆₆N₄O₈

There total 19 articles about C₅₀H₆₆N₄O₈ 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:

: 98990-28-4
C₃₆H₄₈N₂O₆

: 98977-24-3
C₅₀H₆₆N₄O₈

Guidance literature:: Multi-step reaction with 3 steps

1: cyclohexene / 10percent Pd/C / ethanol / 6.5 h / Heating

2: 85.4 percent / glacial acetic acid / 1 h / 80 °C

3: KOH/H₂O / propan-1-ol / 3 h / Heating

With potassium hydroxide; water; acetic acid; cyclohexene; palladium on activated charcoal; In propan-1-ol; ethanol;
DOI:10.1021/jo00233a011

Reference yield:

: 51829-43-7
1,4-dihydroxymethyl-2,5-dimethoxybenzaldehyde

: 98977-24-3
C₅₀H₆₆N₄O₈

Guidance literature:: Multi-step reaction with 5 steps

1: 1.) DMSO/(COCl)2, 2.)Et₃N / 1.) methylene chloride, -78 deg C, 15 min, 2.) methylene chloride, from -78 deg C to RT

2: K₂CO₃ / dioxane / Heating

3: cyclohexene / 10percent Pd/C / ethanol / 6.5 h / Heating

4: 85.4 percent / glacial acetic acid / 1 h / 80 °C

5: KOH/H₂O / propan-1-ol / 3 h / Heating

With potassium hydroxide; oxalyl dichloride; water; potassium carbonate; acetic acid; dimethyl sulfoxide; triethylamine; cyclohexene; palladium on activated charcoal; In 1,4-dioxane; propan-1-ol; ethanol;
DOI:10.1021/jo00233a011

Reference yield:

: 7310-97-6
2,5-dimethoxyterephthalaldehyde

: 98977-24-3
C₅₀H₆₆N₄O₈

Guidance literature:: Multi-step reaction with 4 steps

1: K₂CO₃ / dioxane / Heating

2: cyclohexene / 10percent Pd/C / ethanol / 6.5 h / Heating

3: 85.4 percent / glacial acetic acid / 1 h / 80 °C

4: KOH/H₂O / propan-1-ol / 3 h / Heating

With potassium hydroxide; water; potassium carbonate; acetic acid; cyclohexene; palladium on activated charcoal; In 1,4-dioxane; propan-1-ol; ethanol;
DOI:10.1021/jo00233a011