C₂₆H₃₂N₄O₄S

Base Information

Chemical Name:C₂₆H₃₂N₄O₄S
CAS No.:1374858-99-7
Molecular Formula:C₂₆H₃₂N₄O₄S
Molecular Weight:496.63
Hs Code.:

C<sub>26</sub>H<sub>32</sub>N<sub>4</sub>O<sub>4</sub>S

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 C₂₆H₃₂N₄O₄S

Chemical Property:

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Technology Process of C₂₆H₃₂N₄O₄S

There total 8 articles about C₂₆H₃₂N₄O₄S 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:

: 1374858-21-5
5-amino-3-cyclohexyl-1,2-thiazole-4-carboxamide

: 1374859-12-7
C₁₆H₂₁NO₄

: 1374858-99-7
C₂₆H₃₂N₄O₄S

Guidance literature:: With iodine; In N,N-dimethyl acetamide; at 130 ℃; for 1h;
DOI:10.1016/j.bmcl.2012.03.025

Reference yield:

: 450-83-9
4-fluoro-2-methoxybenzaldehyde

: 1374858-99-7
C₂₆H₃₂N₄O₄S

Guidance literature:: Multi-step reaction with 2 steps

1: potassium carbonate / dimethyl sulfoxide / 80 - 120 °C

2: iodine / N,N-dimethyl acetamide / 1 h / 130 °C

With iodine; potassium carbonate; In N,N-dimethyl acetamide; dimethyl sulfoxide;
DOI:10.1016/j.bmcl.2012.03.025

Reference yield:

: 553672-03-0
[cyclohexyl(hydroxy)methylidene]propanedinitrile

: 1374858-99-7
C₂₆H₃₂N₄O₄S

Guidance literature:: Multi-step reaction with 6 steps

1: trichlorophosphate / Reflux

2: ammonium hydroxide / 0.5 h / 20 °C

3: hydrogen sulfide; triethylamine / benzene

4: dihydrogen peroxide / methanol / 50 °C

5: sulfuric acid / 0.5 h / 80 °C

6: iodine / N,N-dimethyl acetamide / 1 h / 130 °C

With ammonium hydroxide; sulfuric acid; hydrogen sulfide; dihydrogen peroxide; iodine; triethylamine; trichlorophosphate; In methanol; N,N-dimethyl acetamide; benzene;
DOI:10.1016/j.bmcl.2012.03.025