C₂₆H₂₈N₄O₄S₂

Base Information

Chemical Name:C₂₆H₂₈N₄O₄S₂
CAS No.:124820-90-2
Molecular Formula:C₂₆H₂₈N₄O₄S₂
Molecular Weight:524.665
Hs Code.:

C<sub>26</sub>H<sub>28</sub>N<sub>4</sub>O<sub>4</sub>S<sub>2</sub>

Synonyms:

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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 C₂₆H₂₈N₄O₄S₂

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Technology Process of C₂₆H₂₈N₄O₄S₂

There total 11 articles about C₂₆H₂₈N₄O₄S₂ 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:

: 124820-89-9
<4.4.4>propella-3,6-dien-2-one

: 124820-90-2
C₂₆H₂₈N₄O₄S₂

Guidance literature:: Multi-step reaction with 2 steps

1: 28 percent / K₂CrO₄ / acetic acid; acetic anhydride / 1.) 2 h, room temperature, 2.) 4 h, 40 deg C, 3.) 4 d, room temperature

2: conc. hydrochloric acid / methanol

With hydrogenchloride; potassium chromate; In methanol; acetic anhydride; acetic acid;
DOI:10.1021/jo00292a040

Reference yield:

: 124820-88-8
(4aR,8aR)-8a-(2-Oxo-propyl)-1,3,4,5,8,8a-hexahydro-2H-naphthalene-4a-carbaldehyde

: 124820-90-2
C₂₆H₂₈N₄O₄S₂

Guidance literature:: Multi-step reaction with 3 steps

1: 1.48 g / NaOH / ethanol / 3 h / Ambient temperature

2: 28 percent / K₂CrO₄ / acetic acid; acetic anhydride / 1.) 2 h, room temperature, 2.) 4 h, 40 deg C, 3.) 4 d, room temperature

3: conc. hydrochloric acid / methanol

With hydrogenchloride; sodium hydroxide; potassium chromate; In methanol; ethanol; acetic anhydride; acetic acid;
DOI:10.1021/jo00292a040

Reference yield:

: 124820-85-5
methyl cis-9-acetonyl-Δ²-octalin-10-carboxylate

: 124820-90-2
C₂₆H₂₈N₄O₄S₂

Guidance literature:: Multi-step reaction with 7 steps

1: 96 percent / p-toluenesulfonic acid monohydrate / CH₂Cl₂ / 192 h / Ambient temperature

2: 97 percent / LiAlH₄ / diethyl ether / 0.5 h

3: 3.26 g / pyridinium chlorochromate / CH₂Cl₂ / 0.42 h

4: 2.34 g / pyridinium p-toluenesulfonate / acetone; H₂O / 1.5 h / Heating

5: 1.48 g / NaOH / ethanol / 3 h / Ambient temperature

6: 28 percent / K₂CrO₄ / acetic acid; acetic anhydride / 1.) 2 h, room temperature, 2.) 4 h, 40 deg C, 3.) 4 d, room temperature

7: conc. hydrochloric acid / methanol

With hydrogenchloride; sodium hydroxide; potassium chromate; lithium aluminium tetrahydride; pyridinium p-toluenesulfonate; toluene-4-sulfonic acid; pyridinium chlorochromate; In methanol; diethyl ether; ethanol; dichloromethane; water; acetic anhydride; acetic acid; acetone;
DOI:10.1021/jo00292a040