Cas 864515-08-2,3-chloro-5,6-dimethyl-2-{[(2,2,2-trifluoroacetyl)amino]methyl}-2,5-cyclohexadiene-1,4-dione

864515-08-2

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Basic information

Product Name: 3-chloro-5,6-dimethyl-2-{[(2,2,2-trifluoroacetyl)amino]methyl}-2,5-cyclohexadiene-1,4-dione
Synonyms: 3-chloro-5,6-dimethyl-2-{[(2,2,2-trifluoroacetyl)amino]methyl}-2,5-cyclohexadiene-1,4-dione
CAS NO:864515-08-2
Molecular Formula:
Molecular Weight: 295.646
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: 3-chloro-5,6-dimethyl-2-{[(2,2,2-trifluoroacetyl)amino]methyl}-2,5-cyclohexadiene-1,4-dione(CAS DataBase Reference)
NIST Chemistry Reference: 3-chloro-5,6-dimethyl-2-{[(2,2,2-trifluoroacetyl)amino]methyl}-2,5-cyclohexadiene-1,4-dione(864515-08-2)
EPA Substance Registry System: 3-chloro-5,6-dimethyl-2-{[(2,2,2-trifluoroacetyl)amino]methyl}-2,5-cyclohexadiene-1,4-dione(864515-08-2)

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: 864515-08-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 864515-08-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 8,6,4,5,1 and 5 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 864515-08:
(8*8)+(7*6)+(6*4)+(5*5)+(4*1)+(3*5)+(2*0)+(1*8)=182
182 % 10 = 2
So 864515-08-2 is a valid CAS Registry Number.

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864515-08-2Relevant academic research and scientific papers

A general synthesis of quinone ammonium salts

Wiedenfeld, David,Minton, Mark A.,Glass, David R.,Nesterov, Vladimir N.,Nsamenang, Kila D.,Han, Dong

, p. 1611 - 1618 (2007/10/03)

A three-step procedure has been developed to convert substituted p-dimethoxybenzenes to quinone ammonium salts. Five examples of quinone ammonium salts have been prepared with this procedure. In the first step, the aromatic species is reacted with N-(hydr

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