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1,3,6,8-tetra(propan-2-yl)pyrene is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

24300-95-6

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24300-95-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 24300-95-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,4,3,0 and 0 respectively; the second part has 2 digits, 9 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 24300-95:
(7*2)+(6*4)+(5*3)+(4*0)+(3*0)+(2*9)+(1*5)=76
76 % 10 = 6
So 24300-95-6 is a valid CAS Registry Number.

24300-95-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name 1,3,6,8-tetra(propan-2-yl)pyrene

1.2 Other means of identification

Product number -
Other names 3,5,8,10-(Tetra-isopropyl)pyren

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:24300-95-6 SDS

24300-95-6Downstream Products

24300-95-6Relevant academic research and scientific papers

Isolation and X-ray structural characterization of tetraisopropylpyrene cation radical

Banerjee, Moloy,Vyas, Vijay S.,Lindeman, Sergey V.,Rathore, Rajendra

, p. 1889 - 1891 (2008/12/22)

A practical synthesis of 1,3,6,8-tetraisopropylpyrene and the isolation and X-ray structural characterization of its monomeric cation radical salt are described. The Royal Society of Chemistry.

Formation of sec-Alkylpyrenes by Friedel-Crafts and Cathodic Alkylation Methods. Structure and Spectroscopic Properties of Products. Catalytic Hydrogenation of Pyrene and Some Alkylpyrenes

Berg, Arne,Lam, Joergen,Hansen, Poul Erik

, p. 665 - 677 (2007/10/02)

Friedel-Crafts isopropylation of pyrene in neat isopropyl chloride yielded a series of mono, di, tri, tetra, and pentaisopropylpyrenes.Tetra and pentacyclopentyl- and cyclohexylpyrenes were formed analogously.Cathodic isopropylation by controlled potential electrolysis yielded both fully aromatic and partly hydrogenated isopropylpyrenes.Structure of these compounds, spectroscopic properties and mechanistic aspects of their formation are discussed.The catalytic hydrogenation (Raney nickel) of pyrene and isopropylpyrenes under very mild conditions has also been studied.

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