C₃₈H₅₁N₃O₉S

Base Information

Chemical Name:C₃₈H₅₁N₃O₉S
CAS No.:1025019-24-2
Molecular Formula:C₃₈H₅₁N₃O₉S
Molecular Weight:725.904
Hs Code.:

C<sub>38</sub>H<sub>51</sub>N<sub>3</sub>O<sub>9</sub>S

Synonyms:C₃₈H₅₁N₃O₉S

Suppliers and Price of C₃₈H₅₁N₃O₉S

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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 C₃₈H₅₁N₃O₉S

Chemical Property:

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Technology Process of C₃₈H₅₁N₃O₉S

There total 16 articles about C₃₈H₅₁N₃O₉S 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:

: 1025019-41-3
C₄₄H₅₇N₃O₁₂S

: 1025019-24-2
C₃₈H₅₁N₃O₉S

Guidance literature:: C₄₄H₅₇N₃O₁₂S; With sodium methylate; In methanol; for 0.5h;

With hydrogenchloride; In methanol;

Reference yield:

: 540-36-3
para-difluorobenzene

: 1025019-24-2
C₃₈H₅₁N₃O₉S

Guidance literature:: Multi-step reaction with 10 steps

1.1: aluminum (III) chloride / 16 h / 20 °C / Reflux

2.1: potassium carbonate; tetrabutylammomium bromide / toluene / 24 h / Reflux

2.2: 12 h

2.3: 1.5 h

3.1: boron trifluoride diethyl etherate; triethylsilane / 8 h / 65 °C

4.1: potassium carbonate / acetonitrile; ethanol; water / 5 °C

4.2: 1 h

5.1: sodium hydrogencarbonate; 4-acetylamino-2,2,6,6-tetramethyl-1-piperidinoxy; sodium hypochlorite; sodium bromide / dichloromethane; water / 2 h

6.1: potassium tert-butylate / tetrahydrofuran / 1 h / 0 °C

7.1: hydrogen / 5%-palladium/activated carbon / dichloromethane; ethanol / 2250.23 Torr

8.1: ethanol / 8 h / 120 °C / Sealed tube

9.1: N-ethylmorpholine; / dichloromethane / 1 h / 20 °C

9.2: 0.5 h

10.1: sodium methylate / methanol / 0.5 h

With N-ethylmorpholine;; triethylsilane; aluminum (III) chloride; sodium hypochlorite; boron trifluoride diethyl etherate; 4-acetylamino-2,2,6,6-tetramethyl-1-piperidinoxy; potassium tert-butylate; tetrabutylammomium bromide; hydrogen; sodium methylate; sodium hydrogencarbonate; potassium carbonate; sodium bromide; 5%-palladium/activated carbon; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; toluene; acetonitrile;

Reference yield:

: 1193512-70-7
C₁₃H₂₄O₃S

: 1025019-24-2
C₃₈H₅₁N₃O₉S

Guidance literature:: Multi-step reaction with 9 steps

1.1: potassium carbonate; tetrabutylammomium bromide / toluene / 24 h / Reflux

1.2: 12 h

1.3: 1.5 h

2.1: boron trifluoride diethyl etherate; triethylsilane / 8 h / 65 °C

3.1: potassium carbonate / acetonitrile; ethanol; water / 5 °C

3.2: 1 h

4.1: sodium hydrogencarbonate; 4-acetylamino-2,2,6,6-tetramethyl-1-piperidinoxy; sodium hypochlorite; sodium bromide / dichloromethane; water / 2 h

5.1: potassium tert-butylate / tetrahydrofuran / 1 h / 0 °C

6.1: hydrogen / 5%-palladium/activated carbon / dichloromethane; ethanol / 2250.23 Torr

7.1: ethanol / 8 h / 120 °C / Sealed tube

8.1: N-ethylmorpholine; / dichloromethane / 1 h / 20 °C

8.2: 0.5 h

9.1: sodium methylate / methanol / 0.5 h

With N-ethylmorpholine;; triethylsilane; sodium hypochlorite; boron trifluoride diethyl etherate; 4-acetylamino-2,2,6,6-tetramethyl-1-piperidinoxy; potassium tert-butylate; tetrabutylammomium bromide; hydrogen; sodium methylate; sodium hydrogencarbonate; potassium carbonate; sodium bromide; 5%-palladium/activated carbon; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; toluene; acetonitrile;