Cas 1256347-06-4,[2-methyl-4-(trifluoromethylsulfanyl)phenyl]-(m-tolyl)-S-trifluoromethylsulfonium trifluoromethanesulfonate

1256347-06-4

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Basic information

Product Name: [2-methyl-4-(trifluoromethylsulfanyl)phenyl]-(m-tolyl)-S-trifluoromethylsulfonium trifluoromethanesulfonate
Synonyms:
CAS NO:1256347-06-4
Molecular Formula:
Molecular Weight: 532.472
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: [2-methyl-4-(trifluoromethylsulfanyl)phenyl]-(m-tolyl)-S-trifluoromethylsulfonium trifluoromethanesulfonate(CAS DataBase Reference)
NIST Chemistry Reference: [2-methyl-4-(trifluoromethylsulfanyl)phenyl]-(m-tolyl)-S-trifluoromethylsulfonium trifluoromethanesulfonate(1256347-06-4)
EPA Substance Registry System: [2-methyl-4-(trifluoromethylsulfanyl)phenyl]-(m-tolyl)-S-trifluoromethylsulfonium trifluoromethanesulfonate(1256347-06-4)

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: 1256347-06-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1256347-06-4 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, 0 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 1256347-06:
(9*1)+(8*2)+(7*5)+(6*6)+(5*3)+(4*4)+(3*7)+(2*0)+(1*6)=154
154 % 10 = 4
So 1256347-06-4 is a valid CAS Registry Number.

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1256347-06-4Relevant academic research and scientific papers

Self-immolative reduction of trifluoromethyl sulfoxides promoted by trifluoromethanesulfonic anhydride

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

, p. 5772 - 5776 (2010)

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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