Cas 194222-69-0,(2,6-Dinitro-4-trifluoromethanesulfonyl-phenyl)-trifluoromethanesulfonyl-acetic acid ethyl ester

194222-69-0

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Basic information

Product Name: (2,6-Dinitro-4-trifluoromethanesulfonyl-phenyl)-trifluoromethanesulfonyl-acetic acid ethyl ester
Synonyms: (2,6-Dinitro-4-trifluoromethanesulfonyl-phenyl)-trifluoromethanesulfonyl-acetic acid ethyl ester
CAS NO:194222-69-0
Molecular Formula:
Molecular Weight: 518.325
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: (2,6-Dinitro-4-trifluoromethanesulfonyl-phenyl)-trifluoromethanesulfonyl-acetic acid ethyl ester(CAS DataBase Reference)
NIST Chemistry Reference: (2,6-Dinitro-4-trifluoromethanesulfonyl-phenyl)-trifluoromethanesulfonyl-acetic acid ethyl ester(194222-69-0)
EPA Substance Registry System: (2,6-Dinitro-4-trifluoromethanesulfonyl-phenyl)-trifluoromethanesulfonyl-acetic acid ethyl ester(194222-69-0)

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: 194222-69-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 194222-69-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,9,4,2,2 and 2 respectively; the second part has 2 digits, 6 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 194222-69:
(8*1)+(7*9)+(6*4)+(5*2)+(4*2)+(3*2)+(2*6)+(1*9)=140
140 % 10 = 0
So 194222-69-0 is a valid CAS Registry Number.

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194222-69-0Relevant academic research and scientific papers

A novel synthesis of deactivated benzylic triflones

Goumont, Regis,Faucher, Nicolas,Moutiers, Gilles,Tordeux, Marc,Wakselman, Claude

, p. 691 - 695 (1997)

A two-step synthesis of benzylic triflones, based on the reaction of 2.4.6-trisubstituted phenyl halides 3a-f with the anion of ethyl (trifluoromethanesulfonyl)acetate 1 followed by a decarboxylation reaction, is reported. The structural assignments are s

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