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22398-99-8

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22398-99-8 Usage

Uses

Electronic grade in semiconductor devices, injection lasers, and experimental solar cells.

Definition

A brittle metallic mass, mp 1070C, slightly soluble in mineral acids.

Hazard

Probable carcinogen. See indium.

Check Digit Verification of cas no

The CAS Registry Mumber 22398-99-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,2,3,9 and 8 respectively; the second part has 2 digits, 9 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 22398-99:
(7*2)+(6*2)+(5*3)+(4*9)+(3*8)+(2*9)+(1*9)=128
128 % 10 = 8
So 22398-99-8 is a valid CAS Registry Number.

22398-99-8SDS

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 trifluoromethyl(dichlorofluoromethyl)sulfane

1.2 Other means of identification

Product number -
Other names Dichlorofluoro(trifluoromethylthio)methane

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:22398-99-8 SDS

22398-99-8Downstream Products

22398-99-8Relevant articles and documents

Reactions of trifluoromethylthiocopper with halomethanes

Munavalli,Rossman,Rohrbaugh,Ferguson,Durst

, p. 7 - 13 (2007/10/03)

The reaction of trifluoromethylthiocopper with halomethanes, namely di-and triiodo-, dibromodichloro-, dibromochlorofluoro-, dibromo-difluoro-, bromochlorofluoro-, phenyltrichloro-, bromocyano-and dibromofluoro-methanes, has been investigated in detail. In addition to the expected compounds, the formation of unusual products such as bis (trifluoromethyl) trithiocarbonate, dimethyl (trifluoromethylthio) benzene, bis (trifluoromethylthio) fluoromethane, (trifluoromethylthio) carbonyl fluoride, carbon disulfide, carbon tetrachloride, trifluoromethylthio-benzoate, etc. was observed. In some cases, bis (trifluoromethylthio) mercury has been used instead of trifluoromethylthiocopper. The mechanism of formation of the various products and their mass spectral fragmentation behavior are described.

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