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Benzo[rst]pentaphene-5,8-diyl diacetate is a complex organic compound with the molecular formula C20H12O4. It is a derivative of benzo[rst]pentaphene, a polycyclic aromatic hydrocarbon consisting of five fused benzene rings. The diacetate functional group is present at the 5 and 8 positions of the pentaphene structure, which involves the acetylation of two hydroxyl groups. benzo[rst]pentaphene-5,8-diyl diacetate is known for its potential applications in materials science and as a precursor in the synthesis of various organic compounds. Due to its complex structure and chemical properties, benzo[rst]pentaphene-5,8-diyl diacetate is of interest to researchers in the field of organic chemistry, particularly for its potential use in the development of new materials and pharmaceuticals.

3509-60-2

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3509-60-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 3509-60-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 3,5,0 and 9 respectively; the second part has 2 digits, 6 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 3509-60:
(6*3)+(5*5)+(4*0)+(3*9)+(2*6)+(1*0)=82
82 % 10 = 2
So 3509-60-2 is a valid CAS Registry Number.

3509-60-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name benzo[rst]pentaphene-5,8-diyl diacetate

1.2 Other means of identification

Product number -
Other names 5,8-diacetoxy-benzo[rst]pentaphene

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:3509-60-2 SDS

3509-60-2Downstream Products

3509-60-2Relevant 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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