Cas 111055-13-1,Pyridinium, 1-[2,4-bis[(trifluoromethyl)sulfonyl]phenyl]-4-(dimethylamino)-, chloride

111055-13-1

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Basic information

Product Name: Pyridinium, 1-[2,4-bis[(trifluoromethyl)sulfonyl]phenyl]-4-(dimethylamino)-, chloride
Synonyms:
CAS NO:111055-13-1
Molecular Formula: C15H13F6N2O4S2.Cl
Molecular Weight: 498.855
EINECS: N/A
Product Categories: N/A
Mol File: 111055-13-1.mol
Article Data: 1

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: Pyridinium, 1-[2,4-bis[(trifluoromethyl)sulfonyl]phenyl]-4-(dimethylamino)-, chloride(CAS DataBase Reference)
NIST Chemistry Reference: Pyridinium, 1-[2,4-bis[(trifluoromethyl)sulfonyl]phenyl]-4-(dimethylamino)-, chloride(111055-13-1)
EPA Substance Registry System: Pyridinium, 1-[2,4-bis[(trifluoromethyl)sulfonyl]phenyl]-4-(dimethylamino)-, chloride(111055-13-1)

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: 111055-13-1(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 111055-13-1 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,1,0,5 and 5 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 111055-13:
(8*1)+(7*1)+(6*1)+(5*0)+(4*5)+(3*5)+(2*1)+(1*3)=61
61 % 10 = 1
So 111055-13-1 is a valid CAS Registry Number.

111055-13-1Upstream product

111055-13-1Downstream Products

4980-13-6 1-(2,4-bis-trifluoromethanesulfonyl-phenyl)-piperidine

111055-13-1Relevant articles and documents

N-ARYL-4-DIMETHYLAMINOPYRIDINIUM SALTS AND THEIR ARYLATING CHARACTERISTICS

Vizgert, R. V.,Sheiko, S. G.,Kulishova, T. P.,Pekhtereva, T. M.,Nardekova, V. V.

, p. 166 - 169 (2007/10/02)

Quaternary salts were synthesized from 4-dimethylaminopyridine and benzene derivatives which had been activated by nitro- and trifluoromethylsulfonyl groups.These salts were studied by electronic, PMR, and IR spectroscopy.The synthesized quaternary salts

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