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Phenol, 4-[(4-pyridinylmethylene)amino]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

13160-67-3

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13160-67-3 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 13160-67-3 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 1,3,1,6 and 0 respectively; the second part has 2 digits, 6 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 13160-67:
(7*1)+(6*3)+(5*1)+(4*6)+(3*0)+(2*6)+(1*7)=73
73 % 10 = 3
So 13160-67-3 is a valid CAS Registry Number.

13160-67-3Relevant academic research and scientific papers

Optical devices for the detection of cyanide in water based on ethyl(hydroxyethyl)cellulose functionalized with perichromic dyes

Nandi, Leandro Guarezi,Nicoleti, Celso Rodrigo,Marini, Vanderléia Gava,Bellettini, Ismael Casagrande,Valandro, Silvano Rodrigo,Cavalheiro, Carla Cristina Schmitt,Machado, Vanderlei Gageiro

, p. 1548 - 1556 (2017)

Films of three polymers, based on ethyl(hydroxyethyl)cellulose functionalized with protonated perichromic dyes, were used for anion sensing. The polymer functionalized with protonated Brooker's merocyanine acts as a chromogenic/fluorogenic system for the

Synthesis, characterization, and crystal structure analysis of Zn(II) and Cd(II) coordination compounds containing 4-((pyridin-4-ylmethylene)amino)phenol Schiff-base ligand

Flanagan, Keith J.,Hajiashrafi, Taraneh,Kubicki, Maciej,Salehi, Shiva,Senge, Mathias O.

, (2020)

Zn(II) and Cd(II) coordination compounds containing 4-((pyridin-4-ylmethylene)amino)phenol ligands were synthesized and then characterized using spectroscopic techniques and single crystal X-ray crystallography. The molecular structure and crystal packing of these complexes, as well as the crystal packing of coordination complexes based on 4-substituted-1-(pyridin-4-yl)methanimine ligand, retrieved from Cambridge Structural Database (CSD), were investigated using structural, Hirshfeld surface analyses, and theoretical calculations. The crystal structure of these coordination complexes is governed by a combination of π···π stacking, C–H···π, O–H?N, and C–H···X hydrogen bonding interactions. This study provides further insight into the understanding of the role of weak non-covalent interactions in the crystal structure of group IIB containing Schiff-base ligand coordination compounds.

Synthesis and phase transition behaviours of a homologous series of pyridine symmetrical dimers

Ong, Lay-Khoon,Ha, Sie-Tiong,Yeap, Guan-Yeow

, p. 6151 - 6155 (2013)

A series of symmetrical dimers bearing heterocyclic ring, a,w-bis-(4-pyridine-4-methylideneaminoxy) alkanes, were prepared and all the members are differed by the alkyl spacer length (CnH2n, where n = 6, 8, 10, 12). Differential scanning calorimetry and p

Synthesis and characterization of a pyridine-containing Schiff base oligomer

Demir,Kaya,Sacak

, p. 1852 - 1855 (2006)

The oligomer of 4-(4-pyridylmethylideneimino)phenol was formed during oxidative polycondensation in aqueous alkaline medium using oxygen as the oxidant. Optimum conditions of the oxidative polycondensation and the main parameters of the process were found

Solid-state supramolecular architectures of a series of Hg(II) halide coordination compounds based on hydroxyl-substituted Schiff base ligands

Hajiashrafi, Taraneh,Salehi, Shiva,Kubicki, MacIej,Bauzá, Antonio,Frontera, Antonio,Flanagan, Keith J.,Senge, Mathias O.

, p. 6301 - 6312 (2019/11/02)

Crystal engineering of coordination complexes has become an important research domain of modern inorganic chemistry. Herein, six Hg(ii) coordination compounds containing 2-((pyridin-3-ylmethylene)amino)phenol and 4-((pyridin-4-ylmethylene)amino)phenol lig

A new facile method for preparation of heterocyclic α-iminonitriles and α-oxoacetic acid from heterocyclic aldehydes, p-aminophenol, and sodium cyanide

Jursic, Branko S.,Douelle, Frederic,Bowdy, Katherine,Stevens, Edwin D.

, p. 5361 - 5365 (2007/10/03)

Very efficient, simple, and high yield procedures for the transformation of heterocyclic aldehydes into heterocyclic methylidene-p-hydroxyanilines, heterocyclic α-iminonitriles, and finally into heterocyclic α-oxoacetic acids were described. Considering that many of these compounds have biological activity, the synthetic methodology was optimized using readily available, inexpensive starting materials, and the purification of the product involved only simple crystallization.

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