C₃₄H₃₄N₆O₆S₄

Base Information

Chemical Name:C₃₄H₃₄N₆O₆S₄
CAS No.:1399362-75-4
Molecular Formula:C₃₄H₃₄N₆O₆S₄
Molecular Weight:750.945
Hs Code.:

C<sub>34</sub>H<sub>34</sub>N<sub>6</sub>O<sub>6</sub>S<sub>4</sub>

Synonyms:C₃₄H₃₄N₆O₆S₄

Suppliers and Price of C₃₄H₃₄N₆O₆S₄

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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 C₃₄H₃₄N₆O₆S₄

Chemical Property:

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Technology Process of C₃₄H₃₄N₆O₆S₄

There total 14 articles about C₃₄H₃₄N₆O₆S₄ 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:

: 1391396-84-1
C₃₅H₃₆N₆O₆S₄

: 1399362-75-4
C₃₄H₃₄N₆O₆S₄

Guidance literature:: C₃₅H₃₆N₆O₆S₄; With lithium hydroxide; In methanol; dichloromethane; at 20 ℃; for 8h;

In methanol; dichloromethane; water; pH=1; Acidic conditions;
DOI:10.1016/j.tetlet.2012.05.105

Reference yield:

: 1391396-62-5
C₁₉H₂₈N₄O₃S₃

: 1399362-75-4
C₃₄H₃₄N₆O₆S₄

Guidance literature:: Multi-step reaction with 5 steps

1.1: potassium hydrogencarbonate / 1,2-dimethoxyethane / 16 h / 20 °C / Inert atmosphere

1.2: 3 h / 0 °C / Inert atmosphere

2.1: ammonium hydroxide / methanol; water / 20 °C / Sonication

3.1: Lawessons reagent / benzene / 5 h / Inert atmosphere; Reflux

4.1: potassium hydrogencarbonate / 1,2-dimethoxyethane / 16 h / 20 °C / Inert atmosphere

4.2: 3 h / 0 °C / Inert atmosphere

4.3: 3 h / 20 °C / Inert atmosphere

5.1: lithium hydroxide / methanol; dichloromethane / 8 h / 20 °C

5.2: pH 1 / Acidic conditions

With Lawessons reagent; ammonium hydroxide; potassium hydrogencarbonate; lithium hydroxide; In methanol; 1,2-dimethoxyethane; dichloromethane; water; benzene; 1.1: Hantzsch thiazole synthesis / 1.2: Hantzsch thiazole synthesis / 4.1: Hantzsch thiazole synthesis / 4.2: Hantzsch thiazole synthesis / 4.3: Hantzsch thiazole synthesis;
DOI:10.1016/j.tetlet.2012.05.105

Reference yield:

: 1391396-63-6
C₂₄H₃₂N₄O₅S₃

: 1399362-75-4
C₃₄H₃₄N₆O₆S₄

Guidance literature:: Multi-step reaction with 4 steps

1.1: ammonium hydroxide / methanol; water / 20 °C / Sonication

2.1: Lawessons reagent / benzene / 5 h / Inert atmosphere; Reflux

3.1: potassium hydrogencarbonate / 1,2-dimethoxyethane / 16 h / 20 °C / Inert atmosphere

3.2: 3 h / 0 °C / Inert atmosphere

3.3: 3 h / 20 °C / Inert atmosphere

4.1: lithium hydroxide / methanol; dichloromethane / 8 h / 20 °C

4.2: pH 1 / Acidic conditions

With Lawessons reagent; ammonium hydroxide; potassium hydrogencarbonate; lithium hydroxide; In methanol; 1,2-dimethoxyethane; dichloromethane; water; benzene; 3.1: Hantzsch thiazole synthesis / 3.2: Hantzsch thiazole synthesis / 3.3: Hantzsch thiazole synthesis;
DOI:10.1016/j.tetlet.2012.05.105