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Dibenzo[a,i]pyrene[5,8]quinone is a complex organic compound with the molecular formula C22H10O2. It is a derivative of dibenzo[a,i]pyrene, a polycyclic aromatic hydrocarbon (PAH) known for its environmental persistence and potential carcinogenicity. The quinone structure in DIBENZO[A,I]PYRENE[5,8]QUINONE is characterized by the presence of two oxygen atoms bonded to adjacent carbon atoms, forming a C=C-O-O-C=C arrangement. This specific chemical modification can alter the compound's reactivity and biological activity compared to its parent PAH. Dibenzo[a,i]pyrene[5,8]quinone is of interest in chemical research due to its potential applications in the synthesis of other complex molecules and for studying the effects of PAHs and their derivatives on environmental and human health.

3302-52-1

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3302-52-1 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3302-52-1 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,3,0 and 2 respectively; the second part has 2 digits, 5 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 3302-52:
(6*3)+(5*3)+(4*0)+(3*2)+(2*5)+(1*2)=51
51 % 10 = 1
So 3302-52-1 is a valid CAS Registry Number.
InChI:InChI=1/C24H14O2/c25-23-17-7-3-1-5-13(17)15-9-10-16-14-6-2-4-8-18(14)24(26)20-12-11-19(23)21(15)22(16)20/h1-13,17H

3302-52-1SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 19, 2017

Revision Date: Aug 19, 2017

1.Identification

1.1 GHS Product identifier

Product name Benzo(rst)pentaphene-5,8-dione

1.2 Other means of identification

Product number -
Other names 3,4,9,10-Dibenzpyren-5,8-chinon

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:3302-52-1 SDS

3302-52-1Relevant academic research and scientific papers

One-Electron Oxidation of Dibenzopyrenes by Manganic Acetate

Cremonesi, Paolo,Hietbrink, Bruce,Rogan, Eleanor G.,Cavalieri, Ercole L.

, p. 3309 - 3312 (2007/10/02)

The dibenzopyrenes (DBPs) are carcinogenic polycyclic aromatic hydrocarbons (PAH) found as environmental pollutants.DBP is the most potent carcinogenic PAH ever tested.To investigate the bioactivation of DBPs by one-electron oxidation, oxidation of DBP, DBP, DBP, DBP, and anthanthrene with Mn(OAc)3 was conducted and compared to that of benzopyrene (BP).All five DBPs produced monoacetoxy derivatives, and all of them except DBP also produced diacetoxy derivatives.Kinetic studies of the formation of monoacetoxy and diacetoxy derivatives of DBPs were carried out and the results were compared to those of the parent compound BP.DBP was similar to BP.DBP reacted inefficiently to form monoacetoxy and diacetoxy products.The other three DBPs resembled one another.These results provide preliminary essential information for studies of the bioactivation of the very potent carcinogen DBP to form DNA adducts.

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