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C30H37N3O4S

Base Information
  • Chemical Name:C30H37N3O4S
  • CAS No.:1404377-99-6
  • Molecular Formula:C30H37N3O4S
  • Molecular Weight:535.707
  • Hs Code.:
C<sub>30</sub>H<sub>37</sub>N<sub>3</sub>O<sub>4</sub>S

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Chemical Property of C30H37N3O4S
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Technology Process of C30H37N3O4S

There total 27 articles about C30H37N3O4S 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:
Guidance literature:
Multi-step reaction with 22 steps
1.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 20 °C
2.1: 1,1,3,3-Tetramethyldisiloxane / (Ph3P)2IrCl(CO) / toluene / 2 h / 20 °C
3.1: hydroquinone / acetonitrile / 95 °C
4.1: methyl p-toluene sulfonate / water / 2 h / 110 °C
4.2: 4 h / 95 °C
5.1: hydrogen / rhodium contaminated with carbon / tetrahydrofuran / 7 h / 20 °C / 760.05 Torr
6.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 20 °C
7.1: diisobutylaluminium hydride / dichloromethane / 2 h / -78 °C
7.2: Cooling with ice
8.1: triphenylphosphine / dichloromethane / 0.33 h / Cooling with ice
8.2: 0.33 h / Cooling with ice
9.1: n-butyllithium / hexane; tetrahydrofuran / -78 °C
9.2: 1 h / Cooling with ice
10.1: pyridine / methanol / 20 °C
11.1: iodine / acetonitrile / 3 h
12.1: potassium phosphate / bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide; water / 80 °C / Inert atmosphere
13.1: trifluoroacetic acid / chloroform
14.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; ammonium chloride / water
15.1: hydrogenchloride; hydrogen / palladium on activated charcoal / water; tetrahydrofuran
16.1: 1H-imidazole / N,N-dimethyl-formamide
17.1: Lawessons reagent / tetrahydrofuran
18.1: ethanol / Molecular sieve
19.1: tetrabutyl ammonium fluoride; acetic acid / water; tetrahydrofuran
20.1: sodium hypochlorite; sodium chlorite; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical / acetonitrile; water / Phosphate buffer
21.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / water
22.1: sodium hydroxide / ethanol; water; tetrahydrofuran
With Lawessons reagent; pyridine; 1H-imidazole; hydrogenchloride; sodium hypochlorite; sodium chlorite; potassium phosphate; n-butyllithium; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; 1,1,3,3-Tetramethyldisiloxane; tetrabutyl ammonium fluoride; hydrogen; iodine; diisobutylaluminium hydride; ammonium chloride; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; hydroquinone; methyl p-toluene sulfonate; triphenylphosphine; trifluoroacetic acid; sodium hydroxide; bis-triphenylphosphine-palladium(II) chloride; palladium on activated charcoal; rhodium contaminated with carbon; (Ph3P)2IrCl(CO); In tetrahydrofuran; methanol; ethanol; hexane; dichloromethane; chloroform; water; N,N-dimethyl-formamide; toluene; acetonitrile;
Guidance literature:
Multi-step reaction with 21 steps
1.1: 1,1,3,3-Tetramethyldisiloxane / (Ph3P)2IrCl(CO) / toluene / 2 h / 20 °C
2.1: hydroquinone / acetonitrile / 95 °C
3.1: methyl p-toluene sulfonate / water / 2 h / 110 °C
3.2: 4 h / 95 °C
4.1: hydrogen / rhodium contaminated with carbon / tetrahydrofuran / 7 h / 20 °C / 760.05 Torr
5.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 20 °C
6.1: diisobutylaluminium hydride / dichloromethane / 2 h / -78 °C
6.2: Cooling with ice
7.1: triphenylphosphine / dichloromethane / 0.33 h / Cooling with ice
7.2: 0.33 h / Cooling with ice
8.1: n-butyllithium / hexane; tetrahydrofuran / -78 °C
8.2: 1 h / Cooling with ice
9.1: pyridine / methanol / 20 °C
10.1: iodine / acetonitrile / 3 h
11.1: potassium phosphate / bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide; water / 80 °C / Inert atmosphere
12.1: trifluoroacetic acid / chloroform
13.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; ammonium chloride / water
14.1: hydrogenchloride; hydrogen / palladium on activated charcoal / water; tetrahydrofuran
15.1: 1H-imidazole / N,N-dimethyl-formamide
16.1: Lawessons reagent / tetrahydrofuran
17.1: ethanol / Molecular sieve
18.1: tetrabutyl ammonium fluoride; acetic acid / water; tetrahydrofuran
19.1: sodium hypochlorite; sodium chlorite; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical / acetonitrile; water / Phosphate buffer
20.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / water
21.1: sodium hydroxide / ethanol; water; tetrahydrofuran
With Lawessons reagent; pyridine; 1H-imidazole; hydrogenchloride; sodium hypochlorite; sodium chlorite; potassium phosphate; n-butyllithium; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; 1,1,3,3-Tetramethyldisiloxane; tetrabutyl ammonium fluoride; hydrogen; iodine; diisobutylaluminium hydride; ammonium chloride; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; hydroquinone; methyl p-toluene sulfonate; triphenylphosphine; trifluoroacetic acid; sodium hydroxide; bis-triphenylphosphine-palladium(II) chloride; palladium on activated charcoal; rhodium contaminated with carbon; (Ph3P)2IrCl(CO); In tetrahydrofuran; methanol; ethanol; hexane; dichloromethane; chloroform; water; N,N-dimethyl-formamide; toluene; acetonitrile;
Guidance literature:
Multi-step reaction with 19 steps
1.1: methyl p-toluene sulfonate / water / 2 h / 110 °C
1.2: 4 h / 95 °C
2.1: hydrogen / rhodium contaminated with carbon / tetrahydrofuran / 7 h / 20 °C / 760.05 Torr
3.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / N,N-dimethyl-formamide / 20 °C
4.1: diisobutylaluminium hydride / dichloromethane / 2 h / -78 °C
4.2: Cooling with ice
5.1: triphenylphosphine / dichloromethane / 0.33 h / Cooling with ice
5.2: 0.33 h / Cooling with ice
6.1: n-butyllithium / hexane; tetrahydrofuran / -78 °C
6.2: 1 h / Cooling with ice
7.1: pyridine / methanol / 20 °C
8.1: iodine / acetonitrile / 3 h
9.1: potassium phosphate / bis-triphenylphosphine-palladium(II) chloride / N,N-dimethyl-formamide; water / 80 °C / Inert atmosphere
10.1: trifluoroacetic acid / chloroform
11.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol; ammonium chloride / water
12.1: hydrogenchloride; hydrogen / palladium on activated charcoal / water; tetrahydrofuran
13.1: 1H-imidazole / N,N-dimethyl-formamide
14.1: Lawessons reagent / tetrahydrofuran
15.1: ethanol / Molecular sieve
16.1: tetrabutyl ammonium fluoride; acetic acid / water; tetrahydrofuran
17.1: sodium hypochlorite; sodium chlorite; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical / acetonitrile; water / Phosphate buffer
18.1: 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; benzotriazol-1-ol / water
19.1: sodium hydroxide / ethanol; water; tetrahydrofuran
With Lawessons reagent; pyridine; 1H-imidazole; hydrogenchloride; sodium hypochlorite; sodium chlorite; potassium phosphate; n-butyllithium; 2,2,6,6-Tetramethyl-1-piperidinyloxy free radical; tetrabutyl ammonium fluoride; hydrogen; iodine; diisobutylaluminium hydride; ammonium chloride; benzotriazol-1-ol; acetic acid; 1-ethyl-(3-(3-dimethylamino)propyl)-carbodiimide hydrochloride; methyl p-toluene sulfonate; triphenylphosphine; trifluoroacetic acid; sodium hydroxide; bis-triphenylphosphine-palladium(II) chloride; palladium on activated charcoal; rhodium contaminated with carbon; In tetrahydrofuran; methanol; ethanol; hexane; dichloromethane; chloroform; water; N,N-dimethyl-formamide; acetonitrile;
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