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2-(3-phenylpropyl)isothiazolo<5,4-b>pyridine-3(2H)-thione

Base Information
  • Chemical Name:2-(3-phenylpropyl)isothiazolo<5,4-b>pyridine-3(2H)-thione
  • CAS No.:154344-34-0
  • Molecular Formula:C15H14N2S2
  • Molecular Weight:286.422
  • Hs Code.:
2-(3-phenylpropyl)isothiazolo<5,4-b>pyridine-3(2H)-thione

Synonyms:

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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 2-(3-phenylpropyl)isothiazolo<5,4-b>pyridine-3(2H)-thione
Chemical Property:
Purity/Quality:
Safty Information:
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Technology Process of 2-(3-phenylpropyl)isothiazolo<5,4-b>pyridine-3(2H)-thione

There total 20 articles about 2-(3-phenylpropyl)isothiazolo<5,4-b>pyridine-3(2H)-thione 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 35 steps
1: ethanol / Heating
2: I2; NaHCO3 / ethanol
3: Lawesson's reagent / toluene / 0.5 h / Heating
4: H2S / ethanol / pH 7.4
5: I2; NaHCO3 / ethanol
6: Hg(OAc)2; AcOH / CHCl3 / 0.5 h / 20 °C
7: H2S / ethanol / pH 7.4
8: 90 percent / Lawesson's reagent / toluene / 0.5 h / Heating
9: ethanol / Heating
10: I2; NaHCO3 / ethanol
11: Lawesson's reagent / toluene / 0.5 h / Heating
12: Hg(OAc)2; AcOH / CHCl3 / 0.5 h / 20 °C
13: H2S / ethanol / pH 7.4
14: 90 percent / Lawesson's reagent / toluene / 0.5 h / Heating
15: ethanol / Heating
16: 90 percent / Lawesson's reagent / toluene / 0.5 h / Heating
17: ethanol / Heating
18: I2; NaHCO3 / ethanol
19: Lawesson's reagent / toluene / 0.5 h / Heating
20: Hg(OAc)2; AcOH / CHCl3 / 0.5 h / 20 °C
21: H2S / ethanol / pH 7.4
22: 90 percent / Lawesson's reagent / toluene / 0.5 h / Heating
23: ethanol / Heating
24: I2; NaHCO3 / ethanol
25: Lawesson's reagent / toluene / 0.5 h / Heating
26: H2S / ethanol / pH 7.4
27: I2; NaHCO3 / ethanol
28: Hg(OAc)2; AcOH / CHCl3 / 0.5 h / 20 °C
29: H2S / ethanol / pH 7.4
30: 90 percent / Lawesson's reagent / toluene / 0.5 h / Heating
31: ethanol / Heating
32: I2; NaHCO3 / ethanol
33: Lawesson's reagent / toluene / 0.5 h / Heating
34: H2S / ethanol / pH 7.4
35: I2; NaHCO3 / ethanol
With Lawessons reagent; hydrogen sulfide; mercury(II) diacetate; iodine; sodium hydrogencarbonate; acetic acid; In ethanol; chloroform; toluene;
DOI:10.1016/S0014-827X(00)00084-7
Guidance literature:
Multi-step reaction with 17 steps
1: Lawesson's reagent / toluene / 0.5 h / Heating
2: Hg(OAc)2; AcOH / CHCl3 / 0.5 h / 20 °C
3: H2S / ethanol / pH 7.4
4: 90 percent / Lawesson's reagent / toluene / 0.5 h / Heating
5: ethanol / Heating
6: I2; NaHCO3 / ethanol
7: Lawesson's reagent / toluene / 0.5 h / Heating
8: H2S / ethanol / pH 7.4
9: I2; NaHCO3 / ethanol
10: Hg(OAc)2; AcOH / CHCl3 / 0.5 h / 20 °C
11: H2S / ethanol / pH 7.4
12: 90 percent / Lawesson's reagent / toluene / 0.5 h / Heating
13: ethanol / Heating
14: I2; NaHCO3 / ethanol
15: Lawesson's reagent / toluene / 0.5 h / Heating
16: H2S / ethanol / pH 7.4
17: I2; NaHCO3 / ethanol
With Lawessons reagent; hydrogen sulfide; mercury(II) diacetate; iodine; sodium hydrogencarbonate; acetic acid; In ethanol; chloroform; toluene;
DOI:10.1016/S0014-827X(00)00084-7
Guidance literature:
Multi-step reaction with 11 steps
1: Lawesson's reagent / toluene / 0.5 h / Heating
2: H2S / ethanol / pH 7.4
3: I2; NaHCO3 / ethanol
4: Hg(OAc)2; AcOH / CHCl3 / 0.5 h / 20 °C
5: H2S / ethanol / pH 7.4
6: 90 percent / Lawesson's reagent / toluene / 0.5 h / Heating
7: ethanol / Heating
8: I2; NaHCO3 / ethanol
9: Lawesson's reagent / toluene / 0.5 h / Heating
10: H2S / ethanol / pH 7.4
11: I2; NaHCO3 / ethanol
With Lawessons reagent; hydrogen sulfide; mercury(II) diacetate; iodine; sodium hydrogencarbonate; acetic acid; In ethanol; chloroform; toluene;
DOI:10.1016/S0014-827X(00)00084-7
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