Cas 1256347-10-0,4-bromophenyl-[4-(trifluoromethylsulfanyl)phenyl]-S-trifluoromethylsulfonium trifluoromethanesulfonate

1256347-10-0

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Basic information

Product Name: 4-bromophenyl-[4-(trifluoromethylsulfanyl)phenyl]-S-trifluoromethylsulfonium trifluoromethanesulfonate
Synonyms:
CAS NO:1256347-10-0
Molecular Formula:
Molecular Weight: 583.314
EINECS: N/A
Product Categories: N/A

Chemical Properties

Melting Point: N/A
Boiling Point: N/A
Flash Point: N/A
Appearance: N/A
Density: N/A
Refractive Index: N/A
Storage Temp.: N/A
Solubility: N/A
CAS DataBase Reference: 4-bromophenyl-[4-(trifluoromethylsulfanyl)phenyl]-S-trifluoromethylsulfonium trifluoromethanesulfonate(CAS DataBase Reference)
NIST Chemistry Reference: 4-bromophenyl-[4-(trifluoromethylsulfanyl)phenyl]-S-trifluoromethylsulfonium trifluoromethanesulfonate(1256347-10-0)
EPA Substance Registry System: 4-bromophenyl-[4-(trifluoromethylsulfanyl)phenyl]-S-trifluoromethylsulfonium trifluoromethanesulfonate(1256347-10-0)

Safety Data

Hazard Codes: N/A
Statements: N/A
Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 1256347-10-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1256347-10-0 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,5,6,3,4 and 7 respectively; the second part has 2 digits, 1 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1256347-10:
(9*1)+(8*2)+(7*5)+(6*6)+(5*3)+(4*4)+(3*7)+(2*1)+(1*0)=150
150 % 10 = 0
So 1256347-10-0 is a valid CAS Registry Number.

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1256347-10-0Relevant academic research and scientific papers

Self-immolative reduction of trifluoromethyl sulfoxides promoted by trifluoromethanesulfonic anhydride

MacE, Yohan,Blazejewski, Jean-Claude,Pradet, Charlotte,Magnier, Emmanuel

supporting information; experimental part, p. 5772 - 5776 (2011/01/04)

We investigated the behavior of the extensively used system trifluoromethanesulfonic anhydride/sulfoxide in the absence of any added nucleophilic species. We show here, with the help of 19F NMR spectroscopy, that in the case of trifluoromethyl

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