C₄₃H₆₈N₆O₇S

Base Information

Chemical Name:C₄₃H₆₈N₆O₇S
CAS No.:1303556-61-7
Molecular Formula:C₄₃H₆₈N₆O₇S
Molecular Weight:813.115
Hs Code.:

C<sub>43</sub>H<sub>68</sub>N<sub>6</sub>O<sub>7</sub>S

Synonyms:C₄₃H₆₈N₆O₇S

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Chemical Property of C₄₃H₆₈N₆O₇S

Chemical Property:

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Technology Process of C₄₃H₆₈N₆O₇S

There total 9 articles about C₄₃H₆₈N₆O₇S 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:

: 505-18-0
2,3,4,5-tetrahydropyridine

: 1303556-61-7
C₄₃H₆₈N₆O₇S

Guidance literature:: Multi-step reaction with 5 steps

1.1: trifluoroacetic acid / methanol; ethanol / 15.5 h

1.2: 1.5 h

2.1: methanol / 2 h

2.2: 0.17 h

2.3: 9 h

3.1: trifluoroacetic acid / tetrahydrofuran; water / 36 h / 20 °C

4.1: lithium hydroxide / tetrahydrofuran; water / 8 h / 0 - 20 °C

5.1: 2,3,4,5,6-pentafluorophenol; diisopropyl-carbodiimide / dichloromethane / 4 h / 0 - 20 °C

5.2: 20 °C

With 2,3,4,5,6-pentafluorophenol; trifluoroacetic acid; lithium hydroxide; diisopropyl-carbodiimide; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; 1.1: Ugi condensation / 2.1: Ugi condensation / 2.2: Ugi condensation / 2.3: Ugi condensation;
DOI:10.1021/ja2022027

Reference yield:

: (1R,3R)-2-(3-tert-butoxycarbonylamino-1-hydroxy-4-methylpentyl)thiazole-4-carboxylic acid ethyl ester

: 1303556-61-7
C₄₃H₆₈N₆O₇S

Guidance literature:: Multi-step reaction with 6 steps

1.1: 1H-imidazole / N,N-dimethyl-formamide / 0 - 20 °C

2.1: trifluoroacetic acid / dichloromethane / 4 h / 0 °C

3.1: methanol / 2 h

3.2: 0.17 h

3.3: 9 h

4.1: trifluoroacetic acid / tetrahydrofuran; water / 36 h / 20 °C

5.1: lithium hydroxide / tetrahydrofuran; water / 8 h / 0 - 20 °C

6.1: 2,3,4,5,6-pentafluorophenol; diisopropyl-carbodiimide / dichloromethane / 4 h / 0 - 20 °C

6.2: 20 °C

With 1H-imidazole; 2,3,4,5,6-pentafluorophenol; trifluoroacetic acid; lithium hydroxide; diisopropyl-carbodiimide; In tetrahydrofuran; methanol; dichloromethane; water; N,N-dimethyl-formamide; 3.1: Ugi condensation / 3.2: Ugi condensation / 3.3: Ugi condensation;
DOI:10.1021/ja2022027

Reference yield:

: 1101195-49-6
(1S,2S)-2-methyl-1-(4-methyl-2,6,7-trioxabicyclo[2.2.2]oct-1-yl)butyl isocyanide

: 1303556-61-7
C₄₃H₆₈N₆O₇S

Guidance literature:: Multi-step reaction with 5 steps

1.1: trifluoroacetic acid / methanol; ethanol / 15.5 h

1.2: 1.5 h

2.1: methanol / 2 h

2.2: 0.17 h

2.3: 9 h

3.1: trifluoroacetic acid / tetrahydrofuran; water / 36 h / 20 °C

4.1: lithium hydroxide / tetrahydrofuran; water / 8 h / 0 - 20 °C

5.1: 2,3,4,5,6-pentafluorophenol; diisopropyl-carbodiimide / dichloromethane / 4 h / 0 - 20 °C

5.2: 20 °C

With 2,3,4,5,6-pentafluorophenol; trifluoroacetic acid; lithium hydroxide; diisopropyl-carbodiimide; In tetrahydrofuran; methanol; ethanol; dichloromethane; water; 1.1: Ugi condensation / 2.1: Ugi condensation / 2.2: Ugi condensation / 2.3: Ugi condensation;
DOI:10.1021/ja2022027