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7275-44-7

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7275-44-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7275-44-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,2,7 and 5 respectively; the second part has 2 digits, 4 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 7275-44:
(6*7)+(5*2)+(4*7)+(3*5)+(2*4)+(1*4)=107
107 % 10 = 7
So 7275-44-7 is a valid CAS Registry Number.

7275-44-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 18, 2017

Revision Date: Aug 18, 2017

1.Identification

1.1 GHS Product identifier

Product name 4-[2-(4-oxopent-2-en-2-ylamino)ethylamino]pent-3-en-2-one

1.2 Other means of identification

Product number -
Other names Ethylenediaminebisacetoacetamide

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:7275-44-7 SDS

7275-44-7Relevant articles and documents

β-Enaminones over recyclable nano-CoFe2O4: a highly efficient solvent-free green protocol

Eidi, Esmaiel,Kassaee, Mohamad Z.,Cummings, Peter T.

, p. 5787 - 5799 (2018/05/14)

Abstract: β-Enaminone and its derivatives have emerged among the finest bioactive intermediates. High yields of several β-enaminones (86–97%) are achieved through treatment of substituted aromatic and aliphatic amines with cyclic/acyclic 1,3-diketones, over the magnetically separable cobalt ferrite nanoparticles (CoFe2O4 NPs). The latter was prepared upon co-precipitation. Its purity, fine crystallinity, elemental distributions, morphology, magnetic features, and thermal stability were confirmed by Fourier transform infrared, X-ray diffraction, energy dispersive X-ray spectrometry, scanning electron microscopy, vibrating sample magnetometry, and thermal gravimetric analysis analyses. Thus, CoFe2O4 NPs acted as an excellent green heterogeneous nanocatalyst for synthesis of β-enaminones and gave good recyclability, while showing insignificant loss of their activity. Graphical Abstract: [Figure not available: see fulltext.].

Synthesis and structural characterization of β-ketoiminate-stabilized gallium hydrides for chemical vapor deposition applications

Marchand, Peter,Pugh, David,Parkin, Ivan P.,Carmalt, Claire J.

supporting information, p. 10503 - 10513 (2014/08/18)

Bis-β-ketoimine ligands of the form [(CH2) n{N(H)C(Me)-CHC(Me)=O}2] (LnH2, n=2, 3 and 4) were employed in the formation of a range of gallium complexes [Ga(Ln)X] (X=Cl, Me, H), which were characterised by NMR spectroscopy, mass spectrometry and single-crystal X-ray diffraction analysis. The β-ketoimine ligands have also been used for the stabilisation of rare gallium hydride species [Ga(Ln)H] (n=2 (7); n=3 (8)), which have been structurally characterised for the first time, confirming the formation of five-coordinate, monomeric species. The stability of these hydrides has been probed through thermal analysis, revealing stability at temperatures in excess of 200C. The efficacy of all the gallium β-ketoiminate complexes as molecular precursors for the deposition of gallium oxide thin films by chemical vapour deposition (CVD) has been investigated through thermogravimetric analysis and deposition studies, with the best results being found for a bimetallic gallium methyl complex [L3{GaMe2}2] (5) and the hydride [Ga(L3)H] (8). The resulting films (F5 and F8, respectively) were amorphous as-deposited and thus were characterised primarily by XPS, EDXA and SEM techniques, which showed the formation of stoichiometric (F5) and oxygen-deficient (F8) Ga2O3 thin films.

Influence of the structure on the antioxidant activity of tetradentate schiff bases and their copper(II) complexes: Possible mechanisms

Aburas, Najat M.,Stevanovic?, Nikola R.,Milc?ic?, Milos? K.,Lolic?, Aleksandar D.,Natic?, Maja M.,Tes?ic?, Z?ivoslav Lj.,Baos?ic?, Rada M.

, p. 1322 - 1328 (2013/09/24)

The influence of the structure on the antioxidant activity of a series of Schiff bases and their copper(II) complexes as well as possible mechanisms of antioxidant activity were investigated. Schiff bases are derived from the condensation of ethane-1,2-di

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