Cas 87771-58-2,9,14-di-(4'-methylphenyl)-9,9a,10,13,13a,14-hexahydro-9,14-endo-carbonyl-10,13-methanodibenz<a,c>anthracene

87771-58-2

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Basic information

Product Name: 9,14-di-(4'-methylphenyl)-9,9a,10,13,13a,14-hexahydro-9,14-endo-carbonyl-10,13-methanodibenzanthracene
Synonyms:
CAS NO:87771-58-2
Molecular Formula:
Molecular Weight: 502.656
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: 9,14-di-(4'-methylphenyl)-9,9a,10,13,13a,14-hexahydro-9,14-endo-carbonyl-10,13-methanodibenzanthracene(CAS DataBase Reference)
NIST Chemistry Reference: 9,14-di-(4'-methylphenyl)-9,9a,10,13,13a,14-hexahydro-9,14-endo-carbonyl-10,13-methanodibenzanthracene(87771-58-2)
EPA Substance Registry System: 9,14-di-(4'-methylphenyl)-9,9a,10,13,13a,14-hexahydro-9,14-endo-carbonyl-10,13-methanodibenzanthracene(87771-58-2)

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: 87771-58-2(Hazardous Substances Data)

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Check Digit Verification of cas no

The CAS Registry Mumber 87771-58-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 8,7,7,7 and 1 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 87771-58:
(7*8)+(6*7)+(5*7)+(4*7)+(3*1)+(2*5)+(1*8)=182
182 % 10 = 2
So 87771-58-2 is a valid CAS Registry Number.

87771-58-2Upstream product

87771-58-2Downstream Products

87771-61-7 1,4-di-(4'-methylphenyl)triphenylene

87771-58-2Relevant academic research and scientific papers

Polycyclic Aromatic Compounds: Part VIII - A New Synthesis of Polycyclics Containing Phenanthrene Nucleus

Mondal, S.,Bandyopadhyay, T. K.,Bhattacharya, A. J.

, p. 448 - 452 (2007/10/02)

A new series of polycyclic aromatic compounds with phenanthrene nucleus have been prepared.The method involves Diels Alder cycloaddition reaction of 1,3-diaryl-2H-cyclopentaphenanthren-2-one (I) with various dienophiles, viz. bicyclohepta-2,5-di

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