2-Trifluormethylsulfonyl-phenylsulfensaeure-triphenylphosphoranylidenamid

Base Information

Chemical Name:2-Trifluormethylsulfonyl-phenylsulfensaeure-triphenylphosphoranylidenamid
CAS No.:17237-41-1
Molecular Formula:C₂₅H₁₉F₃NO₂PS₂
Molecular Weight:517.532
Hs Code.:

Synonyms:2-Trifluormethylsulfonyl-phenylsulfensaeure-triphenylphosphoranylidenamid

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

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Chemical Property of 2-Trifluormethylsulfonyl-phenylsulfensaeure-triphenylphosphoranylidenamid

Chemical Property:

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Technology Process of 2-Trifluormethylsulfonyl-phenylsulfensaeure-triphenylphosphoranylidenamid

There total 4 articles about 2-Trifluormethylsulfonyl-phenylsulfensaeure-triphenylphosphoranylidenamid 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:

: 17162-42-4
2-Trifluormethylsulfonyl-phenylsulfensaeureamid

: 2526-64-9
dichlorotriphenylphosphorane

: 17237-41-1
2-Trifluormethylsulfonyl-phenylsulfensaeure-triphenylphosphoranylidenamid

Guidance literature:: With triethylamine;

Reference yield:

: 382-70-7
1-chloro-2-(trifluoromethylsulfonyl)benzene

: 17237-41-1
2-Trifluormethylsulfonyl-phenylsulfensaeure-triphenylphosphoranylidenamid

Guidance literature:: Multi-step reaction with 4 steps

1: Na₂S, sulfur / pyridine

2: Cl₂, I₂ / CCl₄

3: aq. NH₃

4: Et₃N

With sodium sulfide; ammonium hydroxide; iodine; chlorine; sulfur; triethylamine; In pyridine; tetrachloromethane;

Reference yield:

: 17162-45-7
Bis-(2-trifluormethylsulfonyl-phenyl)-disulfid

: 17237-41-1
2-Trifluormethylsulfonyl-phenylsulfensaeure-triphenylphosphoranylidenamid

Guidance literature:: Multi-step reaction with 3 steps

1: Cl₂, I₂ / CCl₄

2: aq. NH₃

3: Et₃N

With ammonium hydroxide; iodine; chlorine; triethylamine; In tetrachloromethane;