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1062610-12-1

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1062610-12-1 Usage

General Description

2,4,6-Trifluorophenylsulphur pentafluoride is a chemical compound with the molecular formula C6F5SF5. It is a highly reactive and toxic compound that is used as a fluorinating agent in organic synthesis. It is a colorless liquid under standard conditions and has a distinct pungent odor. Due to its highly fluorinated nature, it is capable of introducing fluorine atoms into organic molecules, making it a valuable reagent in the field of fluorine chemistry. However, it is important to handle this compound with caution due to its toxicity and reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 1062610-12-1 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,0,6,2,6,1 and 0 respectively; the second part has 2 digits, 1 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 1062610-12:
(9*1)+(8*0)+(7*6)+(6*2)+(5*6)+(4*1)+(3*0)+(2*1)+(1*2)=101
101 % 10 = 1
So 1062610-12-1 is a valid CAS Registry Number.

1062610-12-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name pentafluoro-(2,4,6-trifluorophenyl)-λ<sup>6</sup>-sulfane

1.2 Other means of identification

Product number -
Other names 1-(Pentafluorothio)-2,4,6-trifluorobenzene

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:1062610-12-1 SDS

1062610-12-1Downstream Products

1062610-12-1Relevant articles and documents

Discovery of practical production processes for arylsulfur pentafluorides and their higher homologues, bis- and tris(sulfur pentafluorides): Beginning of a new era of "super-trifluoromethyl" arene chemistry and its industry

Umemoto, Teruo,Garrick, Lloyd M.,Saito, Norimichi

, p. 461 - 471 (2012/07/01)

Various arylsulfur pentafluorides, ArSF5, have long been desired in both academic and industrial areas, and ArSF5 compounds have attracted considerable interest in many areas such as medicines, agrochemicals, and other new materials, since the highly stable SF5 group is considered a "super-trifluoromethyl group" due to its significantly higher electronegativity and lipophilicity. This article describes the first practical method for the production of various arylsulfur pentafluorides and their higher homologues, bis- and tris(sulfur pentafluorides), from the corresponding diaryl disulfides or aryl thiols. The method consists of two steps: (Step 1) treatment of a diaryl disulfide or an aryl thiol with chlorine in the presence of an alkali metal fluoride, and (step 2) treatment of the resulting arylsulfur chlorotetrafluoride with a fluoride source, such as ZnF2, HF, and Sb(III/V) fluorides. The intermediate arylsulfur chlorotetrafluorides were isolated by distillation or recrystallization and characterized. The aspects of these new reactions are revealed and reaction mechanisms are discussed. As the method offers considerable improvement over previous methods in cost, yield, practicality, applicability, and large-scale production, the new processes described here can be employed as the first practical methods for the economical production of various arylsulfur pentafluorides and their higher homologues, which could then open up a new era of "super-trifluoromethyl" arene chemistry and its applications in many areas.

PROCESS FOR PRODUCING ARYLSULFUR PENTAFLUORIDES

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Page/Page column 17, (2008/12/07)

Novel processes for preparing arylsulfur pentafluorides are disclosed. Processes include reacting at least one aryl sulfur compound with a halogen and a fluoro salt to form an arylsulfur halotetrafluoride. The arylsulfur halotetrafluoride is reacted with a fluoride source to form a target arylsulfur pentafluoride.

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