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Hydrazinecarbothioamide, 2-[2-(hydroxyimino)-1-methylpropylidene]-N-phenyl- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

56566-64-4

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56566-64-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 56566-64-4 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,6,5,6 and 6 respectively; the second part has 2 digits, 6 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 56566-64:
(7*5)+(6*6)+(5*5)+(4*6)+(3*6)+(2*6)+(1*4)=154
154 % 10 = 4
So 56566-64-4 is a valid CAS Registry Number.

56566-64-4SDS

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 3-hydroxyiminobutanone 4-phenylthiosemicarbazone

1.2 Other means of identification

Product number -
Other names diacetylmonoxime-N(4)-phenylthiosemicarbazone

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:56566-64-4 SDS

56566-64-4Relevant academic research and scientific papers

Ruthenium(II) complexes of thiosemicarbazones: Synthesis, X-ray crystal structures, spectroscopy, electrochemistry, DFT studies and fluoride sensing properties

Ghosh, Bipinbihari,Adak, Piyali,Naskar, Subhendu,Pakhira, Bholanath,Mitra, Partha,Dinda, Rupam,Chattopadhyay, Shyamal Kumar

, p. 1 - 14 (2017)

Six Ru(II) complexes with formula [Ru(terpy)(L)]X (L = tridentate N,N,S?donor thiosemicarbazone ligands, X = PF6?) have been synthesized and characterized by using standard analytical and spectroscopic techniques. The X-ray crystal structures of the complexes [Ru(terpy)(L2)]PF6(2) and [Ru(terpy)(L3)]PF6(3) have been determined. It was found that during complexation the hydroxyimino functionality of the parent ligands is converted to imine, which participates in coordination through the N-atom. The complexes are found to undergo two quasi-reversible oxidations on the positive side of the potential window (0 to +0.8 V) and three successive quasi-reversible/irreversible reductions on the negative side of the potential window (0 to ?2 V). The fluoride sensing properties of all the complexes have been studied in solution using absorption spectra and1H NMR studies, as well as by cyclic voltammetric (CV) measurements. From the absorption titration studies the association constants and detection limit values of fluoride by the complexes have been determined. The association constant values were found to be reasonably high (logKa> 5) for complexes 3–6, and these values are one order of magnitude greater than those observed for the corresponding free thiosemicarbazones. Selective fluoride sensing by these complexes is also signaled by the development of vivid colors, visible with the naked eye.

DNA binding and cleavage activities of cationic dinuclear copper(II) and nickel(II) Complexes with novel oximethiosemicarbazones

Haribabu,Hussain Reddy

experimental part, p. 996 - 1001 (2011/09/12)

Complexes of Cu(II) and Ni(II) with novel type of ligands, viz., diacetylmonoximethiosemicarbazone, diacetylmonoxime-N(4)- methylthiosemicarbazone, diacetylmonoxime-N(4)-ethylthiosemicarbazone and diacetylmonoxime-N(4)-phenylthiosemicarbazone have been synthesized and characterized based on molar conductance, magnetic moment, electronic, IR and ESR spectral data. Electrochemical behaviour of these complexes is investigated by cyclic voltammetric studies. The binding properties of these complexes with calf-thymus DNA have been investigated using absorption spectrophotometry. Cleavage activity of these complexes has been investigated on double stranded pBR 322 plasmid DNA by gel electrophoresis experiments in the absence and in the presence of oxidant.

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