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4-[3-(4-oxopentan-2-ylideneamino)propylimino]pentan-2-one is a complex organic compound with the molecular formula C14H21N3O3. It is characterized by a pentan-2-one core, which is a five-carbon ketone with a carbonyl group at the second position. The compound features a 4-oxopentan-2-ylidene moiety, which is a key structural element that contributes to its reactivity and properties. This molecule is of interest in the field of organic chemistry, particularly in the synthesis of various pharmaceuticals and chemical intermediates. Its unique structure allows for potential applications in the development of new compounds with specific biological activities.

6310-78-7

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6310-78-7 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 6310-78-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,3,1 and 0 respectively; the second part has 2 digits, 7 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 6310-78:
(6*6)+(5*3)+(4*1)+(3*0)+(2*7)+(1*8)=77
77 % 10 = 7
So 6310-78-7 is a valid CAS Registry Number.

6310-78-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name N,N'-bis(1-methyl-3-oxobutylidene)-1,3-propanediamine

1.2 Other means of identification

Product number -
Other names Bis-acetylaceton-trimethylendiimin

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:6310-78-7 SDS

6310-78-7Downstream Products

6310-78-7Relevant academic research and scientific papers

Binary roles of schiff bases as capping agent and precursor for synthesis of metallic nickel ultrafine nanoparticles

Motahari,Mozdianfard,Soofivand,Salavati-Niasari

, p. 1449 - 1456 (2015)

This study focused on the synthesis and characterization of nickel nanoparticles by simple precipitation method. The various Schiff bases such as ethylenediamine (acacen), 1,3-propylenediamine (acacpn), and butane-1,4-diamine (acacbn) acetyl acetonate were prepared and were used for preparing of nickel-Schiff base complexes and then, these complexes as precursor were reduced in the presence of KBH4, for the first time. In addition, the anti-aggregation effect of prepared Schiff bases was compared with common surfactants and results demonstrated that the huge ligands can be considered as novel surfactants. The obtained nickel nanoparticles were characterized by XRD, TEM, HRTEM, FT-IR, SEM, and EDS.

Copper(II) complexes with Schiff bases: Structures and thermal behavior

Dorovskikh,Kuratieva,Tkachev,Trubin,Stabnikov,Morozova

, p. 1067 - 1074 (2014)

Ligands with Schiff bases are obtained in the condensation of propylenediamine (pda) or 2,2-dimethylpropylenediamine (dmpda) with acetylacetone (Hacac) in the 1:2 molar ratio. The ligands are characterized by the elemental analysis methods, T melt = 90-92 °C for pda(Hacac)2 (pda(acac)2 is N,N′-propylene-bis(acetylacetoniminato) (2-)), T melt = 84-86 °C for dmpda(Hacac)2 (dmpda(acac)2 is N,N′-2,2-dimethylpropylene-bis(acetylacetoniminato) (2-)). The tautomerism of the ligands is established by the single crystal X-ray diffraction (XRD) analysis, IR spectroscopy, and 1H, 13C NMR spectrometry. The synthesized complexes [Cu(pda(acac)2)] (1), T melt = 121-122 °C and [Cu(dmpda(acac)2)] (2), T melt = 156-158 °C are studied by the XRD method. In both complexes, copper atoms have a planar square geometry, and the chelate bond lengths and angles are: Cu-O ≈ Cu-N 1.903(2)-1.942(3) ?, ∠O-Cu-N = 94.44(12)-94.99(12)° for 1 and Cu-O ≈ Cu-N 1.909(1)-1.943(2) ?, ∠O-Cu-N = 94.63(6)° for 2. By the thermogravimetric method it is found that both complexes can be passed practically quantitatively into the gas phase.

Aldimine and Ketimine Derivatives of Titanium(IV)

Sharma, R. K.,Singh, R. V.,Tandon, J. P.

, p. 378 - 379 (2007/10/02)

Reactions of titanium isopropoxyde with aldimines and ketamines in equimolar ratios have been carried out.The products have been obtained in almost quantitative yields and characterized on the basis of elemental analyses, molecular weight determinations, exchange reactions, conductance measurements and IR, PMR and UV spectral data.

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