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Benzene, 1-(chloromethyl)-4-methoxy-2-[[4-(methylsulfonyl)phenyl]thio]-

Base Information Edit
  • Chemical Name:Benzene, 1-(chloromethyl)-4-methoxy-2-[[4-(methylsulfonyl)phenyl]thio]-
  • CAS No.:98190-63-7
  • Molecular Formula:C15H15ClO3S2
  • Molecular Weight:342.867
  • Hs Code.:
  • Mol file:98190-63-7.mol
Benzene, 1-(chloromethyl)-4-methoxy-2-[[4-(methylsulfonyl)phenyl]thio]-

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Suppliers and Price of Benzene, 1-(chloromethyl)-4-methoxy-2-[[4-(methylsulfonyl)phenyl]thio]-
Supply Marketing:Edit
Business phase:
The product has achieved commercial mass production*data from LookChem market partment
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Total 1 raw suppliers
Chemical Property of Benzene, 1-(chloromethyl)-4-methoxy-2-[[4-(methylsulfonyl)phenyl]thio]- Edit
Chemical Property:
Purity/Quality:

99% *data from raw suppliers

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Technology Process of Benzene, 1-(chloromethyl)-4-methoxy-2-[[4-(methylsulfonyl)phenyl]thio]-

There total 10 articles about Benzene, 1-(chloromethyl)-4-methoxy-2-[[4-(methylsulfonyl)phenyl]thio]- 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 7 steps
1: 24 percent / charcoal, FeCl3*6H2O, N2H4*H2O / ethanol / 4 h / Heating; standing 2 weeks
2: 1) HCl, NaNO2, 2) potassium ethyl xanthate, Na2CO3 / 1) H2O, 0 to 2 deg C, 30 min, 2) 40 deg C, 30 min
3: 86 percent / K2CO3, Cu / dimethylformamide / 5 h / 140 °C
4: 82 percent / SOCl2 / pyridine / 6 h / Heating
5: 85 percent / 5 h / Heating
6: 88 percent / NaBH4, BF3*O(C2H5)2 / tetrahydrofuran / r.t., 5 h, reflux, 2 h
7: HCl / 0.5 h / 60 - 70 °C
With hydrogenchloride; sodium tetrahydroborate; thionyl chloride; boron trifluoride diethyl etherate; potassium ethyl xanthogenate; iron(III) chloride; copper; sodium carbonate; potassium carbonate; pyrographite; hydrazine hydrate; sodium nitrite; In tetrahydrofuran; pyridine; ethanol; N,N-dimethyl-formamide;
DOI:10.1135/cccc19850519
Guidance literature:
Multi-step reaction with 7 steps
1: 75 percent / aq. NH3 / 20 h / 200 - 210 °C / 1) autoclave; 2) standing 48 h,
2: 1) HCl, NaNO2, 2) potassium ethyl xanthate, Na2CO3 / 1) H2O, 0 to 2 deg C, 30 min, 2) 40 deg C, 30 min
3: 86 percent / K2CO3, Cu / dimethylformamide / 5 h / 140 °C
4: 82 percent / SOCl2 / pyridine / 6 h / Heating
5: 85 percent / 5 h / Heating
6: 88 percent / NaBH4, BF3*O(C2H5)2 / tetrahydrofuran / r.t., 5 h, reflux, 2 h
7: HCl / 0.5 h / 60 - 70 °C
With hydrogenchloride; ammonium hydroxide; sodium tetrahydroborate; thionyl chloride; boron trifluoride diethyl etherate; potassium ethyl xanthogenate; copper; sodium carbonate; potassium carbonate; sodium nitrite; In tetrahydrofuran; pyridine; N,N-dimethyl-formamide;
DOI:10.1135/cccc19850519
Guidance literature:
Multi-step reaction with 6 steps
1: 1) HCl, NaNO2, 2) potassium ethyl xanthate, Na2CO3 / 1) H2O, 0 to 2 deg C, 30 min, 2) 40 deg C, 30 min
2: 86 percent / K2CO3, Cu / dimethylformamide / 5 h / 140 °C
3: 82 percent / SOCl2 / pyridine / 6 h / Heating
4: 85 percent / 5 h / Heating
5: 88 percent / NaBH4, BF3*O(C2H5)2 / tetrahydrofuran / r.t., 5 h, reflux, 2 h
6: HCl / 0.5 h / 60 - 70 °C
With hydrogenchloride; sodium tetrahydroborate; thionyl chloride; boron trifluoride diethyl etherate; potassium ethyl xanthogenate; copper; sodium carbonate; potassium carbonate; sodium nitrite; In tetrahydrofuran; pyridine; N,N-dimethyl-formamide;
DOI:10.1135/cccc19850519
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