Cas 112079-84-2,2,5-Cyclohexadien-1-one, 2,4,6-tris(1,1-dimethylethyl)-4-[(5'-phenyl[1,1':3',1''-terphenyl]-2'-yl)amino ]-

112079-84-2

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Basic information

Product Name: 2,5-Cyclohexadien-1-one, 2,4,6-tris(1,1-dimethylethyl)-4-[(5'-phenyl[1,1':3',1''-terphenyl]-2'-yl)amino ]-
Synonyms:
CAS NO:112079-84-2
Molecular Formula: C42H47NO
Molecular Weight: 581.841
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: 2,5-Cyclohexadien-1-one, 2,4,6-tris(1,1-dimethylethyl)-4-[(5'-phenyl[1,1':3',1''-terphenyl]-2'-yl)amino ]-(CAS DataBase Reference)
NIST Chemistry Reference: 2,5-Cyclohexadien-1-one, 2,4,6-tris(1,1-dimethylethyl)-4-[(5'-phenyl[1,1':3',1''-terphenyl]-2'-yl)amino ]-(112079-84-2)
EPA Substance Registry System: 2,5-Cyclohexadien-1-one, 2,4,6-tris(1,1-dimethylethyl)-4-[(5'-phenyl[1,1':3',1''-terphenyl]-2'-yl)amino ]-(112079-84-2)

Safety Data

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Safety Statements: N/A
WGK Germany:
RTECS:
HazardClass: N/A
PackingGroup: N/A
Hazardous Substances Data: 112079-84-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 112079-84-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,2,0,7 and 9 respectively; the second part has 2 digits, 8 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 112079-84:
(8*1)+(7*1)+(6*2)+(5*0)+(4*7)+(3*9)+(2*8)+(1*4)=102
102 % 10 = 2
So 112079-84-2 is a valid CAS Registry Number.

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112079-84-2Relevant academic research and scientific papers

OXYDATION D'AMINES AROMATIQUES PRIMAIRES EN PRESENCE DU RADICAL TRITERTIOBUTYL-2,4,6 PHENOXYLE

Hedayatullah, Mir

, p. 311 - 324 (2007/10/02)

The trapping of anilino radicals generated by a mild dehydrogenation of primary aromatic amines, at 20 deg C, in homogenous medium or in two-phase system, by 2,4,6-tritertiobutylphenoxy radical is carried out and the structures of the corresponding C-N or C-C coupling products are established by spectral data (IR, UV, RMN 1H).

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