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Tetrabenz[a,c,h,j]anthracene is a polycyclic aromatic hydrocarbon (PAH) consisting of four fused benzene rings and four additional carbon atoms, forming a complex molecular structure. It is a synthetic chemical compound with the molecular formula C26H16 and is characterized by its high stability and resistance to degradation. TETRABENZ[A,C,H,J]ANTHRACENE is known for its potential carcinogenic and mutagenic properties, making it a subject of concern in environmental and health studies. Due to its persistence and toxicity, tetrabenz[a,c,h,j]anthracene is monitored in various environmental matrices, and efforts are made to limit its release into the environment.

215-11-2

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215-11-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 215-11-2 includes 6 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 3 digits, 2,1 and 5 respectively; the second part has 2 digits, 1 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 215-11:
(5*2)+(4*1)+(3*5)+(2*1)+(1*1)=32
32 % 10 = 2
So 215-11-2 is a valid CAS Registry Number.
InChI:InChI=1/C30H18/c1-5-13-23-19(9-1)20-10-2-6-14-24(20)28-18-30-26-16-8-4-12-22(26)21-11-3-7-15-25(21)29(30)17-27(23)28/h1-18H

215-11-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 15, 2017

Revision Date: Aug 15, 2017

1.Identification

1.1 GHS Product identifier

Product name Tetrabenz(a,c,h,j)anthracene

1.2 Other means of identification

Product number -
Other names 1,2,3,4,5,6,7,8-Tetrabenzoanthracen

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:215-11-2 SDS

215-11-2Downstream Products

215-11-2Relevant academic research and scientific papers

Synthesis of extended triphenylenes by palladium-catalyzed [2+2+2] cycloaddition of triphenylynes

Romero, Carmen,Pena, Diego,Perez, Dolores,Guitian, Enrique

, p. 5677 - 5684 (2008/03/13)

The synthesis of orttho-(trimethylsilyl)triphenylenyl triflates 7 is described. Fluoride-induced decomposition of these triflates leads to the generation of didehydrotriphenylenes (triphenylynes). 6. These arynes undergo [4+2] cycloadditions with dienes to afford the corresponding Diels-Alder adducts or palladium-catalyzed formal [2+2+2] cycloadditions to afford extended triphenylenes.

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