Cas 80575-84-4,Trifluoro-methanesulfonate1-[(Z)-2-(3-chloro-phenyl)-1-phenyl-vinyl]-4,6-diphenyl-2,3-dihydro-pyridinium;

80575-84-4

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Basic information

Product Name: Trifluoro-methanesulfonate1-[(Z)-2-(3-chloro-phenyl)-1-phenyl-vinyl]-4,6-diphenyl-2,3-dihydro-pyridinium;
Synonyms:
CAS NO:80575-84-4
Molecular Formula:
Molecular Weight: 596.07
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: Trifluoro-methanesulfonate1-[(Z)-2-(3-chloro-phenyl)-1-phenyl-vinyl]-4,6-diphenyl-2,3-dihydro-pyridinium;(CAS DataBase Reference)
NIST Chemistry Reference: Trifluoro-methanesulfonate1-[(Z)-2-(3-chloro-phenyl)-1-phenyl-vinyl]-4,6-diphenyl-2,3-dihydro-pyridinium;(80575-84-4)
EPA Substance Registry System: Trifluoro-methanesulfonate1-[(Z)-2-(3-chloro-phenyl)-1-phenyl-vinyl]-4,6-diphenyl-2,3-dihydro-pyridinium;(80575-84-4)

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: 80575-84-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 80575-84-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,0,5,7 and 5 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 80575-84:
(7*8)+(6*0)+(5*5)+(4*7)+(3*5)+(2*8)+(1*4)=144
144 % 10 = 4
So 80575-84-4 is a valid CAS Registry Number.

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80575-84-4Relevant academic research and scientific papers

Pyridinium Ylides Derived from Pyryliums and Amines and a Novel Rearrangement of 1-Vinyl-1,2-dihydropyridines

Katritzky, Alan R.,Chermprapai, Amornsri,Patel, Ranjan C.,Tarraga-Tomas, Alberto

, p. 492 - 497 (2007/10/02)

1-Benzyl-2,4-diphenylpyridiniums with benzaldehydes give oxazolopyridines which are dehydrated to 1-styryl derivatives.On pyrolysis the 1-styryl-1,2-dihydropyridine 21a gave 2,4,6-triphenylpyridine and m-chlorostyrene by a ring-enlargement-ring-contraction mechanism: this is a general reaction of 1-vinyl-1,2-dihydropyridines.

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