C₈H₅ClF₈OS

Base Information

Chemical Name:C₈H₅ClF₈OS
CAS No.:1594970-70-3
Molecular Formula:C₈H₅ClF₈OS
Molecular Weight:336.633
Hs Code.:

C<sub>8</sub>H<sub>5</sub>ClF<sub>8</sub>OS

Synonyms:C₈H₅ClF₈OS

Suppliers and Price of C₈H₅ClF₈OS

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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 C₈H₅ClF₈OS

Chemical Property:

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Technology Process of C₈H₅ClF₈OS

There total 4 articles about C₈H₅ClF₈OS 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: 92.0%

: 772-53-2
(1,2,2-trifluorovinyloxy)benzene

: 1594970-70-3
C₈H₅ClF₈OS

Guidance literature:: With pentafluorosulfanyl chloride; dibenzoyl peroxide; at 20 - 110 ℃; for 8h; Temperature; Inert atmosphere;
DOI:10.1021/ol500766v

Reference yield:

: 108-95-2,27073-41-2
phenol

: 1594970-70-3
C₈H₅ClF₈OS

Guidance literature:: Multi-step reaction with 3 steps

1.1: potassium hydroxide; tetrabutylammomium bromide / 4 - 10 °C

2.1: potassium hydroxide / methanol / Inert atmosphere

2.2: 250 - 280 °C / Inert atmosphere

3.1: dibenzoyl peroxide; pentafluorosulfanyl chloride / 8 h / 20 - 110 °C / Inert atmosphere

With pentafluorosulfanyl chloride; tetrabutylammomium bromide; potassium hydroxide; dibenzoyl peroxide; In methanol;
DOI:10.1021/ol500766v

Reference yield:

: 100-67-4
potassium phenolate

: 1594970-70-3
C₈H₅ClF₈OS

Guidance literature:: Multi-step reaction with 3 steps

1: 100 °C / Autoclave; Inert atmosphere

2: 240 - 260 °C / Inert atmosphere; Pyrolysis

3: dibenzoyl peroxide; pentafluorosulfanyl chloride / 8 h / 20 - 110 °C / Inert atmosphere

With pentafluorosulfanyl chloride; dibenzoyl peroxide;
DOI:10.1021/ol500766v