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374-10-7

Trifluoromethylsulfur trifluoride, also known as sulfur trifluoride trifluoride or F3SF3, is a highly reactive and toxic chemical compound consisting of one sulfur atom bonded to three fluorine atoms and another sulfur atom bonded to three fluorine atoms. It is a colorless, volatile, and unstable gas with a pungent odor. Trifluoromethylsulfur trifluoride is primarily used in the synthesis of various fluorocarbons and as a fluorinating agent in organic chemistry. Due to its high reactivity, it can react with a wide range of substances, including water, organic compounds, and metals, making it a potentially hazardous material that requires careful handling and storage.

374-10-7

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374-10-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 374-10-7 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 3,7 and 4 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 374-10:
(5*3)+(4*7)+(3*4)+(2*1)+(1*0)=57
57 % 10 = 7
So 374-10-7 is a valid CAS Registry Number.

374-10-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name trifluoro(trifluoromethyl)sulfur(IV)

1.2 Other means of identification

Product number -
Other names Trifluormethylsulfurtrifluorid

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:374-10-7 SDS

374-10-7Relevant articles and documents

BEITRAEGE ZUR CHEMIE DER SCHEFELHALOGENIDE 15. DICHLOR-FLUOR-TRIFLUOROMETHYLSULFURAN, CF3SCl2F

Minkwitz, Rolf,Nass, Ulrike

, p. 393 - 398 (2007/10/02)

The preparation of the sulfurane CF3SCl2F is reported.Upon sublimation of the sulfonium salt CF3SCl2+AsF6- the compounds CF3SCl2F and AsF5 coexist in the gaseous phase.After trapping AsF5 as KAsF6 extremely instable CF3SCl2F is isolated and characterised by IR-, Raman- and 19F-NMR-spectroscopy.

Preparation and Chemical Properties of S-(Trifluoromethyl)-S,N-dihalosulfimides, (Trifluoromethylthio)(thiosulfinyl)amine, and Bis(trifluoromethyldithio)sulfur Diimide

Haas, Alois,Walz, Ruediger

, p. 3248 - 3257 (2007/10/02)

Oxidative halogenation of CF3SN(SiMe3)2 with F2 or Cl2 leads to CF3S(X)=NX (X=F, Cl) (2a, b).During the chlorination process CF3S(Cl)=NSiMe3 (3a) was isolated and characterized as an intermediate.It reacts with CF3SCl to give CF3S(Cl)=NSCF3 (3b) which was also obtained from (CF3S)2NH and Cl2 at -60 deg C.Similarly, CF3S(F)=NSCF3 (3c) was synthesized from (CF3S)2NH and F2 or from CF3SF3 and CF3SNH2. 3a-c decompose already at temperatures 5a, b).Analoguosly, CF3SN=S=NSCF3 (4b) reacts with cyclopentadiene to give 5c.Ringopening takes place during the reaction of + Cl- (6) with Hg(SCF3)2 with formation of CF3SSN=S=NSSCF3 (7) which was also obtained from (CF3SS)2NH and (ClSN)3 in the presence of pyridine.Physical and spectroscopic data of the compounds are reported.

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