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1-formyl-1,2,3,4-tetrahydro-6,7-dimethoxy-4-phenylthioquinoline

Base Information Edit
  • Chemical Name:1-formyl-1,2,3,4-tetrahydro-6,7-dimethoxy-4-phenylthioquinoline
  • CAS No.:250156-30-0
  • Molecular Formula:C18H19NO3S
  • Molecular Weight:329.42
  • Hs Code.:
  • Mol file:250156-30-0.mol
1-formyl-1,2,3,4-tetrahydro-6,7-dimethoxy-4-phenylthioquinoline

Synonyms:1-formyl-1,2,3,4-tetrahydro-6,7-dimethoxy-4-phenylthioquinoline

Suppliers and Price of 1-formyl-1,2,3,4-tetrahydro-6,7-dimethoxy-4-phenylthioquinoline
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The product has achieved commercial mass production*data from LookChem market partment
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Chemical Property of 1-formyl-1,2,3,4-tetrahydro-6,7-dimethoxy-4-phenylthioquinoline Edit
Chemical Property:
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Technology Process of 1-formyl-1,2,3,4-tetrahydro-6,7-dimethoxy-4-phenylthioquinoline

There total 6 articles about 1-formyl-1,2,3,4-tetrahydro-6,7-dimethoxy-4-phenylthioquinoline 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:
With boron trifluoride diethyl etherate; trifluoroacetic anhydride; In benzene; at 20 ℃; for 1h;
DOI:10.1248/cpb.47.1269
Guidance literature:
Multi-step reaction with 4 steps
1: NaI; Na2CO3; TEAB / dioxane / 144 h / Heating
2: Ac2O / 1 h / 60 °C
3: 96 percent / NaIO4 / methanol / 6 h / 20 °C
4: 84 percent / TFAA; BF3*Et2O / benzene / 1 h / 20 °C
With sodium periodate; boron trifluoride diethyl etherate; tetraethylammonium bromide; acetic anhydride; sodium carbonate; trifluoroacetic anhydride; sodium iodide; In 1,4-dioxane; methanol; benzene; 1: Condensation / 2: Formylation / 3: Oxidation / 4: Pummerer reaction;
DOI:10.1248/cpb.47.1269
Guidance literature:
Multi-step reaction with 5 steps
1: 83 percent / SOCl2 / pyridine / 10 h / 110 °C
2: NaI; Na2CO3; TEAB / dioxane / 144 h / Heating
3: Ac2O / 1 h / 60 °C
4: 96 percent / NaIO4 / methanol / 6 h / 20 °C
5: 84 percent / TFAA; BF3*Et2O / benzene / 1 h / 20 °C
With sodium periodate; thionyl chloride; boron trifluoride diethyl etherate; tetraethylammonium bromide; acetic anhydride; sodium carbonate; trifluoroacetic anhydride; sodium iodide; In 1,4-dioxane; pyridine; methanol; benzene; 1: Chlorination / 2: Condensation / 3: Formylation / 4: Oxidation / 5: Pummerer reaction;
DOI:10.1248/cpb.47.1269
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