110210-53-2 Usage
Type of compound
Polycyclic aromatic hydrocarbon (PAH)
Structure
Composed of six fused benzene rings
Substituents
Two isopropyl groups on the 1 and 6 positions
Reactivity
Highly reactive
Toxicity
Toxic and considered a potential human carcinogen
Applications
Primarily used in research and laboratory experiments
Health effects
Can cause damage to DNA, negative impacts on respiratory, reproductive, and immune systems
Safety
Handle with caution and follow safety protocols in laboratory settings
Check Digit Verification of cas no
The CAS Registry Mumber 110210-53-2 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,1,0,2,1 and 0 respectively; the second part has 2 digits, 5 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 110210-53:
(8*1)+(7*1)+(6*0)+(5*2)+(4*1)+(3*0)+(2*5)+(1*3)=42
42 % 10 = 2
So 110210-53-2 is a valid CAS Registry Number.
110210-53-2Relevant academic research and scientific papers
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.
