Cas 1227710-60-2,[(2-hydroxy-4,4-dimethyl-6-oxo-cyclohex-1-enyl)-(2,3,5,6-tetrafluoro-4-trifluoromethylphenyl)]iodonium toluene-4-sulfonate

1227710-60-2

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Basic information

Product Name: [(2-hydroxy-4,4-dimethyl-6-oxo-cyclohex-1-enyl)-(2,3,5,6-tetrafluoro-4-trifluoromethylphenyl)]iodonium toluene-4-sulfonate
Synonyms:
CAS NO:1227710-60-2
Molecular Formula:
Molecular Weight: 654.341
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-hydroxy-4,4-dimethyl-6-oxo-cyclohex-1-enyl)-(2,3,5,6-tetrafluoro-4-trifluoromethylphenyl)]iodonium toluene-4-sulfonate(CAS DataBase Reference)
NIST Chemistry Reference: [(2-hydroxy-4,4-dimethyl-6-oxo-cyclohex-1-enyl)-(2,3,5,6-tetrafluoro-4-trifluoromethylphenyl)]iodonium toluene-4-sulfonate(1227710-60-2)
EPA Substance Registry System: [(2-hydroxy-4,4-dimethyl-6-oxo-cyclohex-1-enyl)-(2,3,5,6-tetrafluoro-4-trifluoromethylphenyl)]iodonium toluene-4-sulfonate(1227710-60-2)

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: 1227710-60-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 1227710-60-2 includes 10 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 7 digits, 1,2,2,7,7,1 and 0 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 1227710-60:
(9*1)+(8*2)+(7*2)+(6*7)+(5*7)+(4*1)+(3*0)+(2*6)+(1*0)=132
132 % 10 = 2
So 1227710-60-2 is a valid CAS Registry Number.

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1227710-60-2Relevant academic research and scientific papers

A versatile and highly reactive polyfluorinated hypervalent iodine (III) compound

Schaefer, Sascha,Wirth, Thomas

supporting information; experimental part, p. 2786 - 2789 (2010/07/06)

(Figure Presented) Hyper-reactive: A highly reactive, fully fluorinated hypervalent iodine reagent (see formula) mediates new transformations (e.g. the one-pot conversion of sulfides to sulfoximines) and serves as a stoichiometric oxidant in well-established reactions (e.g. C-C bond cleavage and the conversion of alcohols into aldehydes).

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