Cas 362011-05-0,5',5'''-bis(2,6-diisopropylphenyl)-2,6,2'''',6''''-tetraisopropyl-m-quinquephenyl-2''-yl amine

362011-05-0

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Basic information

Product Name: 5',5'''-bis(2,6-diisopropylphenyl)-2,6,2'''',6''''-tetraisopropyl-m-quinquephenyl-2''-yl amine
Synonyms: 5',5'''-bis(2,6-diisopropylphenyl)-2,6,2'''',6''''-tetraisopropyl-m-quinquephenyl-2''-yl amine
CAS NO:362011-05-0
Molecular Formula:
Molecular Weight: 886.36
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: 5',5'''-bis(2,6-diisopropylphenyl)-2,6,2'''',6''''-tetraisopropyl-m-quinquephenyl-2''-yl amine(CAS DataBase Reference)
NIST Chemistry Reference: 5',5'''-bis(2,6-diisopropylphenyl)-2,6,2'''',6''''-tetraisopropyl-m-quinquephenyl-2''-yl amine(362011-05-0)
EPA Substance Registry System: 5',5'''-bis(2,6-diisopropylphenyl)-2,6,2'''',6''''-tetraisopropyl-m-quinquephenyl-2''-yl amine(362011-05-0)

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: 362011-05-0(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 362011-05-0 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 3,6,2,0,1 and 1 respectively; the second part has 2 digits, 0 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 362011-05:
(8*3)+(7*6)+(6*2)+(5*0)+(4*1)+(3*1)+(2*0)+(1*5)=90
90 % 10 = 0
So 362011-05-0 is a valid CAS Registry Number.

362011-05-0Upstream product

362011-05-0Downstream Products

362011-05-0Relevant academic research and scientific papers

A novel dendrimer-type m-terphenyl substituent for the kinetic stabilization of highly reactive species

Goto, Kei,Yamamoto, Gaku,Tan, Bo,Okazaki, Renji

, p. 4875 - 4877 (2001)

A novel m-terphenyl-based steric protection group (Bpq group) bearing a dendrimer-type framework was designed and successfully applied to the stabilization of the corresponding N-thiosulfinylaniline and arenesulfenyl iodide. The Bpq group was found to provide a very inert environment for the reactive functionality embedded in its cleft.

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