Cas 15463-88-4,2,6-Di-tert.butyl-4-(3,5-di-tert.butyl-4-oxo-cyclohedien-(2,5)-ylidenamino)-phenolat

15463-88-4

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Basic information

Product Name: 2,6-Di-tert.butyl-4-(3,5-di-tert.butyl-4-oxo-cyclohedien-(2,5)-ylidenamino)-phenolat
Synonyms:
CAS NO:15463-88-4
Molecular Formula:
Molecular Weight: 422.631
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-Di-tert.butyl-4-(3,5-di-tert.butyl-4-oxo-cyclohedien-(2,5)-ylidenamino)-phenolat(CAS DataBase Reference)
NIST Chemistry Reference: 2,6-Di-tert.butyl-4-(3,5-di-tert.butyl-4-oxo-cyclohedien-(2,5)-ylidenamino)-phenolat(15463-88-4)
EPA Substance Registry System: 2,6-Di-tert.butyl-4-(3,5-di-tert.butyl-4-oxo-cyclohedien-(2,5)-ylidenamino)-phenolat(15463-88-4)

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: 15463-88-4(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 15463-88-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,5,4,6 and 3 respectively; the second part has 2 digits, 8 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 15463-88:
(7*1)+(6*5)+(5*4)+(4*6)+(3*3)+(2*8)+(1*8)=114
114 % 10 = 4
So 15463-88-4 is a valid CAS Registry Number.

15463-88-4Upstream product

4610-03-1 2,6-di-tert-butyl-4-(3,5-di-tert-butyl-4-hydroxyphenylimino)-2,5-cyclohexadien-1-one

15463-88-4Downstream Products

15463-88-4Relevant academic research and scientific papers

SPECTRA AND STRUCTURE OF SCREENED PHENOLS, THEIR RADICALS AND IONS

Kotorlenko, L. A.,Aleksandrova, V. S.,Yankovich, V. N.

, p. 501 - 504 (1984)

The vibrational spectra of screened phenols, stable phenoxyl radicals and ions obtained by addition (loss) of the proton to the phenol molecule, and one-electron reduction (oxidation) of the phenoxyl radical, were studied and interpreted.The proton phototransfer between phenol molecules of the same type in frozen aliphatic hydrocarbon solutions was revealed by luminescence.

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