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1932-08-7

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1932-08-7 Usage

General Description

ACENAPHTHENEQUINONE DIOXIME, also known as Acenaphthoquinone dioxime, is a chemical compound with the formula C14H10N2O2. Despite limited available information, it can be inferred that it is possibly utilized in chemical synthesis or research due to its structure containing dioxime and quinone groups. These groups typically imply a range of potential reactions, and quinones are often used in energy processes such as those found in biological systems. However, its precise uses, properties, production methods, and safety measures remain largely undefined in accessible literature. Always exercise caution when handling chemical substances, using appropriate protective measures, and adhering to safety protocols.

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 articles and documents

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.

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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