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62925-34-2

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62925-34-2 Usage

Complex structure

Consists of two nitro groups, two keto groups, and four oxygen atoms bound to a polycyclic aromatic hydrocarbon backbone
Highly reactive and potentially toxic substance
Byproduct of industrial processes involving the combustion of organic materials
Known to have mutagenic and carcinogenic properties
Poses significant environmental and health risks
Production and use are regulated in many countries.

Check Digit Verification of cas no

The CAS Registry Mumber 62925-34-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,2,9,2 and 5 respectively; the second part has 2 digits, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 62925-34:
(7*6)+(6*2)+(5*9)+(4*2)+(3*5)+(2*3)+(1*4)=132
132 % 10 = 2
So 62925-34-2 is a valid CAS Registry Number.
InChI:InChI=1/C14H4N2O8/c17-13-7-1-5(15(19)20)3-9-11(7)12-8(14(18)24-9)2-6(16(21)22)4-10(12)23-13/h1-4H

62925-34-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 12, 2017

Revision Date: Aug 12, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,7-Dinitro-5,10-dioxo-4,9-dioxapyrene

1.2 Other means of identification

Product number -
Other names 2,7-dinitro-5,10-dioxo-4,5,9,10-tetrahydro-4,9-dioxapyrene

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:62925-34-2 SDS

62925-34-2Downstream Products

62925-34-2Relevant articles and documents

Bromination of deactivated polycyclic aromatic nitro compounds

Andrievskii,Gorelik,Linko,Grachev

, p. 1474 - 1481 (2013)

Bromination of 2,7-dinitro-9,10-phenanthrenequinone, 2,5-dinitro-9,10- phenanthrenequinone, and 2,4,7-trinitrofluorenone with bromine in concentrated sulfuric acid in the presence of acetic acid gave, respectively, 4-bromo-2,7-dinitro-9,10-phenanthrenequinone, 2-bromo-4,7-dinitro-9,10- phenanthrenequinone, and 5-bromo-2,4,7-trinitrofluorenone. No bromination occurred in the absence of nitric acid. The same brominated polynitro compounds can be obtained under analogous conditions directly from unsubstituted 9,10-phenanthrenequinone and fluorenone.

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