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ACENAPHTHENEQUINONE DIOXIME, also known as Acenaphthoquinone dioxime, is a chemical compound with the formula C14H10N2O2. It is characterized by the presence of dioxime and quinone groups in its structure, which suggests potential applications in chemical synthesis or research. Although the precise uses, properties, production methods, and safety measures are not well-defined in accessible literature, the presence of these functional groups indicates a range of possible reactions and applications, particularly in energy processes similar to those found in biological systems.

1932-08-7

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1932-08-7 Usage

Uses

Used in Chemical Synthesis:
ACENAPHTHENEQUINONE DIOXIME is used as a chemical intermediate for various synthesis processes due to its dioxime and quinone groups. These groups are known to participate in a range of potential reactions, making it a valuable compound in the development of new chemical products.
Used in Research Applications:
ACENAPHTHENEQUINONE DIOXIME is used as a research compound for studying the properties and reactions of dioxime and quinone groups. Its structure provides opportunities for exploring the behavior of these functional groups in different chemical environments, contributing to the advancement of scientific knowledge in related fields.
Used in Energy Processes:
ACENAPHTHENEQUINONE DIOXIME is used as a component in energy-related research, particularly in biological systems. The quinone group is often involved in energy processes, and the presence of this group in the compound suggests potential applications in the study and development of energy transfer mechanisms.
Safety Measures:
When handling ACENAPHTHENEQUINONE DIOXIME, it is essential to exercise caution and use appropriate protective measures. Adhering to safety protocols is crucial to minimize risks associated with chemical substances. Due to the limited information available, it is recommended to consult with experts and follow established guidelines for safe handling and disposal of such compounds.

Check Digit Verification of cas no

The CAS Registry Mumber 1932-08-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,9,3 and 2 respectively; the second part has 2 digits, 0 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1932-08:
(6*1)+(5*9)+(4*3)+(3*2)+(2*0)+(1*8)=77
77 % 10 = 7
So 1932-08-7 is a valid CAS Registry Number.
InChI:InChI=1/C12H8N2O2/c15-13-11-8-5-1-3-7-4-2-6-9(10(7)8)12(11)14-16/h1-6,13,15H

1932-08-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 11, 2017

Revision Date: Aug 11, 2017

1.Identification

1.1 GHS Product identifier

Product name N-(2-nitrosoacenaphthylen-1-yl)hydroxylamine

1.2 Other means of identification

Product number -
Other names Acenaphthen-1,2-dion-dioxim

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:1932-08-7 SDS

1932-08-7Relevant academic research and scientific papers

High-Throughput Screening of Earth-Abundant Water Reduction Catalysts toward Photocatalytic Hydrogen Evolution

Motz, Rachel N.,Lopato, Eric M.,Connell, Timothy U.,Bernhard, Stefan

supporting information, p. 774 - 781 (2021/02/05)

Noble-metal photosensitizers and water reduction co-catalysts (WRCs) still present the highest activity in homogeneous photocatalytic hydrogen production. The search for earth-abundant alternatives is usually limited by the time required to screen new catalyst combinations; however, here, we utilize newly designed and developed high-throughput photoreactors for the parallel synthesis of novel WRCs and colorimetric screening of hydrogen evolution. This unique approach allowed rapid optimization of photocatalytic water reduction using the organic photosensitizer Eosin Y and the archetypal cobaloxime WRC [Co(GL1)2pyCl], where GL1 is dimethylglyoxime and py is pyridine. Subsequent combinatorial synthesis generated 646 unique cobalt complexes of the type [Co(LL)2pyCl], where LL is a bidentate ligand, that identified promising new WRC candidates for hydrogen production. Density functional theory (DFT) calculations performed on such cobaloxime derivative complexes demonstrated that reactivity depends on hydride affinity. Alkyl-substituted glyoximes were necessary for hydrogen production and showed increased activity when paired with ligands containing strong hydrogen-bond donors.

Potential photoacid generators based on oxime sulfonates

Plater, M. John,Harrison, William T. A.,Killah, Ross

, p. 26 - 33 (2019/06/03)

The bis-oxime of acenaphthenequinone and the mono-oxime of benzil have been sulfonated by reaction with 4-methylbenzenesulfonyl chloride and propylsulfonyl chloride. The four sulfonated oximes were characterised by X-ray single-crystal structure determinations. Some photochemical decompositions were studied using a 6-W 254-nm immersion well lamp in dichloromethane. The 4-methylbenzenesulfonate bis-oxime of acenaphthenequinone and the 4-methylbenzenesulfonate mono-oxime of benzil both give 4-methylbenzenesulfonic acid upon irradiation but not 4-methylbenzenesulfinic acid. Fragmentation pathways are discussed. The possible use of these compounds as photoacid generators in polymer resists and the role of secondary reactions to liberate acid is discussed.

Structural and electronic characterization of multi-electron reduced naphthalene (BIAN) cobaloximes

Williams, Owen M.,Cowley, Alan H.,Rose, Michael J.

, p. 13017 - 13029 (2016/01/09)

Reported here are the syntheses and characterization of cobaloximes that feature a bis(imino)acenaphthene (BIAN) appended ligand. The X-ray crystal structures and spectroscopy (1H NMR or EPR) of the complexes within the series [Co(aqdBF2/

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