C₁₆H₁₆F₂N₆O₄S₂

Base Information

Chemical Name:C₁₆H₁₆F₂N₆O₄S₂
CAS No.:1391916-07-6
Molecular Formula:C₁₆H₁₆F₂N₆O₄S₂
Molecular Weight:458.47
Hs Code.:

C<sub>16</sub>H<sub>16</sub>F<sub>2</sub>N<sub>6</sub>O<sub>4</sub>S<sub>2</sub>

Synonyms:C₁₆H₁₆F₂N₆O₄S₂

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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 C₁₆H₁₆F₂N₆O₄S₂

Chemical Property:

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Technology Process of C₁₆H₁₆F₂N₆O₄S₂

There total 3 articles about C₁₆H₁₆F₂N₆O₄S₂ 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:

: 1391916-05-4
C₁₆H₁₆F₂N₆O₂S₂

: 1391916-06-5
C₁₆H₁₆F₂N₆O₃S₂

: 1391916-07-6
C₁₆H₁₆F₂N₆O₄S₂

Guidance literature:: With 3-chloro-benzenecarboperoxoic acid; In dichloromethane; at 20 ℃; for 0.5h;

Reference yield:

: 3896-29-5
N-(2,6-difluorophenyl)acetamide

: 1391916-06-5
C₁₆H₁₆F₂N₆O₃S₂

: 1391916-07-6
C₁₆H₁₆F₂N₆O₄S₂

Guidance literature:: Multi-step reaction with 6 steps

1: potassium nitrate; sulfuric acid / water / -10 - 20 °C

2: hydrogen / palladium 10% on activated carbon / methanol / 3 h / 10343.2 Torr / Autoclave

3: pyridine / dichloromethane / 16 h / 20 °C

4: hydrogenchloride / ethanol; water / 2 h / 80 °C

5: acetic acid / methanol / 2 h / 50 °C

6: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0.5 h / 20 °C

With pyridine; hydrogenchloride; sulfuric acid; hydrogen; acetic acid; potassium nitrate; 3-chloro-benzenecarboperoxoic acid; palladium 10% on activated carbon; In methanol; ethanol; dichloromethane; water;

Reference yield:

: 25892-08-4
N-(2,6-difluoro-3-nitrophenyl)acetamide

: 1391916-06-5
C₁₆H₁₆F₂N₆O₃S₂

: 1391916-07-6
C₁₆H₁₆F₂N₆O₄S₂

Guidance literature:: Multi-step reaction with 5 steps

1: hydrogen / palladium 10% on activated carbon / methanol / 3 h / 10343.2 Torr / Autoclave

2: pyridine / dichloromethane / 16 h / 20 °C

3: hydrogenchloride / ethanol; water / 2 h / 80 °C

4: acetic acid / methanol / 2 h / 50 °C

5: 3-chloro-benzenecarboperoxoic acid / dichloromethane / 0.5 h / 20 °C

With pyridine; hydrogenchloride; hydrogen; acetic acid; 3-chloro-benzenecarboperoxoic acid; palladium 10% on activated carbon; In methanol; ethanol; dichloromethane; water;