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1,2-diphenyltriphenylene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

79421-23-1

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79421-23-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79421-23-1 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,4,2 and 1 respectively; the second part has 2 digits, 2 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 79421-23:
(7*7)+(6*9)+(5*4)+(4*2)+(3*1)+(2*2)+(1*3)=141
141 % 10 = 1
So 79421-23-1 is a valid CAS Registry Number.

79421-23-1SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,2-diphenyltriphenylene

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:79421-23-1 SDS

79421-23-1Downstream Products

79421-23-1Relevant academic research and scientific papers

Eine Cycloadditions-Cyclodehydrierungs-Route von stilbenoiden zu ausgedehnten aromatischen Kohlenwasserstoffen

Mueller, Markus,Mauermann-Duell, Heike,Wagner, Manfred,Enkelmann, Volker,Muellen, Klaus

, p. 1751 - 1754 (2007/10/02)

Stichworte: Cycloadditionen, Cyclodehydrierungen, Diels-Alder Reaktionen, Graphitausschnitte, Polycyclen

Photochemical Studies. On the Photofragmentation of Substituted 1,2-Dihydrophthalic Anhydrides

Fuchs, Benzion,Scharf, Gad

, p. 5395 - 5398 (2007/10/02)

The irradiation-induced transformations of 4,5-diphenyl-1,2-dihydrophthalic anhydride (2b) as well as those of the 3,6-dimethyl-4,5-diphenyl and 3,4,5,6-tetraphenyl derivatives (2c,d) are elaborated.All undergo photofragmentation, viz., CO + CO2 ejection to give aromatic hydrocarbons, while only 2b also closes electrocyclically to the bicyclohex-5-ene product 5.The quantum yields for fragmentation are indicative in this respect.The rearrangement accompanying the fragmentation of 2d to give 1,2,3,5-tetraphenylbenzene (11) was shown to occur via a triplet excited state, populated by benzene sensitization.

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