methyl 4,5,6,7-tetrafluoro-1-benzyl-3-phenyl-2,3-dihydrobenzo[d]isothiazole-3-carboxylate 1,1-dioxide

Base Information

Chemical Name:methyl 4,5,6,7-tetrafluoro-1-benzyl-3-phenyl-2,3-dihydrobenzo[d]isothiazole-3-carboxylate 1,1-dioxide
CAS No.:1049837-78-6
Molecular Formula:C₂₂H₁₅F₄NO₄S
Molecular Weight:465.425
Hs Code.:

Synonyms:methyl 4,5,6,7-tetrafluoro-1-benzyl-3-phenyl-2,3-dihydrobenzo[d]isothiazole-3-carboxylate 1,1-dioxide

Suppliers and Price of methyl 4,5,6,7-tetrafluoro-1-benzyl-3-phenyl-2,3-dihydrobenzo[d]isothiazole-3-carboxylate 1,1-dioxide

Supply Marketing:

Business phase:: The product has achieved commercial mass production^*data from LookChem market partment

Manufacturers and distributors:

Manufacture/Brand
Chemicals and raw materials
Packaging
price

Total 0 raw suppliers

Chemical Property of methyl 4,5,6,7-tetrafluoro-1-benzyl-3-phenyl-2,3-dihydrobenzo[d]isothiazole-3-carboxylate 1,1-dioxide

Chemical Property:

Purity/Quality:

Safty Information:

Pictogram(s):
Hazard Codes:

MSDS Files:

Useful:

Technology Process of methyl 4,5,6,7-tetrafluoro-1-benzyl-3-phenyl-2,3-dihydrobenzo[d]isothiazole-3-carboxylate 1,1-dioxide

There total 3 articles about methyl 4,5,6,7-tetrafluoro-1-benzyl-3-phenyl-2,3-dihydrobenzo[d]isothiazole-3-carboxylate 1,1-dioxide 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: 85.0%

: 1049837-84-4
methyl 4,5,6,7-tetrafluoro-3-phenyl-2,3-dihydrobenzo[d]isothiazole-3-carboxylate 1,1-dioxide

: 100-39-0
benzyl bromide

: 1049837-78-6
methyl 4,5,6,7-tetrafluoro-1-benzyl-3-phenyl-2,3-dihydrobenzo[d]isothiazole-3-carboxylate 1,1-dioxide

Guidance literature:: With N-benzyl-N,N,N-triethylammonium chloride; potassium carbonate; In acetonitrile; at 25 ℃; for 20h;
DOI:10.1021/jo800930g

Reference yield: 50.0%

: 1049837-76-4
methyl 2-(N-benzyl-2,3,4,5,6-pentafluorophenylsulfonamido)-2-phenylacetate

: 1049837-78-6
methyl 4,5,6,7-tetrafluoro-1-benzyl-3-phenyl-2,3-dihydrobenzo[d]isothiazole-3-carboxylate 1,1-dioxide

Guidance literature:: With 1,8-diazabicyclo[5.4.0]undec-7-ene; In acetonitrile; at 25 ℃;
DOI:10.1021/jo800930g

Reference yield: 32.0%

: 1049837-64-0
methyl 2-(2,3,4,5,6-pentafluorophenylsulfonamido)-2-phenylacetate

: 100-39-0
benzyl bromide

: 1049837-78-6
methyl 4,5,6,7-tetrafluoro-1-benzyl-3-phenyl-2,3-dihydrobenzo[d]isothiazole-3-carboxylate 1,1-dioxide

Guidance literature:: With N-benzyl-N,N,N-triethylammonium chloride; sodium carbonate; In dimethyl sulfoxide; at 50 ℃; for 20h;
DOI:10.1021/jo800930g