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Cyclopent[fg]acenaphthylene-1,2-dione is a complex organic compound with the molecular formula C17H8O2. It is a derivative of acenaphthylene, which is a polycyclic aromatic hydrocarbon consisting of two fused benzene rings. The cyclopent[fg]acenaphthylene-1,2-dione structure features a cyclopentane ring fused to the acenaphthylene core, with two carbonyl groups (C=O) attached to the first and second carbon atoms of the acenaphthylene moiety. Cyclopent[fg]acenaphthylene-1,2-dione is of interest in the field of organic chemistry and may have potential applications in materials science and pharmaceuticals due to its unique structure and properties. However, further research is needed to explore its full potential and understand its behavior in various chemical reactions and applications.

5253-87-2

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5253-87-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 5253-87-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,2,5 and 3 respectively; the second part has 2 digits, 8 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5253-87:
(6*5)+(5*2)+(4*5)+(3*3)+(2*8)+(1*7)=92
92 % 10 = 2
So 5253-87-2 is a valid CAS Registry Number.

5253-87-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name cyclopent<fg>acenaphthylene-1,2-dione

1.2 Other means of identification

Product number -
Other names pyracycloquinone

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:5253-87-2 SDS

5253-87-2Relevant academic research and scientific papers

Highly resilient polyethylene elastomers prepared using α-diimine nickel catalyst with highly conjugated backbone

He, Feng,Wang, Dan,Wu, Anyang,Jiang, Baiyu,Zhang, Zhen,Cheng, Zhenmei,Fu, Zhisheng,Zhang, Qisheng,Fan, Zhiqiang

, (2018)

An α-diimine nickel catalyst (Cat-1) with highly conjugated acenaphthylene backbone was synthesized and used in ethylene polymerization. Compared with typical Brookhart catalyst B-Cat, Cat-1 could produce polyethylene with both higher molecular weight (up to 5.1?×?105?g?mol?1) and branching density (up to 135 branches per 1000 carbons) in good polymerization activity. The polyethylene prepared using Cat-1 with higher molecular weight and branching density possessed exceptional mechanical properties (ultimate tensile strength and elongation at break could reach 12.08?MPa and 1148%) and outstanding elastomeric recovery as compared with the polymer prepared using B-Cat. Cat-1 was synthesized using a simple reaction route and the polymerization conditions were suitable for the industrial polymerization process. The novel nickel catalyst Cat-1 is promising for producing highly resilient polyethylene elastomers industrially.

ORGANIC COMPOUND, THREE-DIMENSIONAL ORGANIC FRAMEWORK FORMED BY USING ORGANIC COMPOUND, SEPARATION SIEVE AND OPTICAL LAYER, WHICH COMPRISE ORGANIC FRAMEWORK, AND OPTICAL DEVICE COMPRISING OPTICAL LAYER AS OPTICAL AMPLIFICATION LAYER

-

, (2019/02/13)

An organic compound, a three-dimensional organic structure formed by using the organic compound, a separation sieve and an optical layer having the organic structure, and an optical device having the optical layer as an optical amplification layer are provided. The organic structure includes a plurality of organic molecules self-assembled by non-covalent bonding. Each of the unit organic molecules has an aromatic ring, a first pair of substituents being connected to immediately adjacent positions of substitutable positions of the aromatic ring, and a second pair of substituents being connected to immediately adjacent positions of remaining substitutable positions of the aromatic ring. The unit organic molecules are self-assembled by van der Waals interaction, London dispersion interaction or hydrogen bonding between the first and the second pairs of the substituents and by pi-pi interactions between the aromatic rings.

Organic compound and 3-dimensional organic framework formed using the same

-

, (2018/07/07)

Provided is a three-dimensional organic framework. The organic framework comprises a plurality of organic molecules which are self-assembled by non-covalent bonds. Each of the organic molecules comprises: a first pair of substituents which are each bound to an aromatic ring and to immediately adjacent positions among substitutable positions of the aromatic ring; and a second pair of substituents which are each bound to immediately adjacent positions among the rest of the substitutable positions. The organic molecules are self-assembled through Van Der Waals interactions, London dispersion interactions, or hydrogen bonding between the first and second pairs of the substituents, and andpi;-andpi; interactions between the aromatic rings.COPYRIGHT KIPO 2018

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