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4-(1,4,7,10-tetrathia-13-aza-cyclopentadec-13-yl)-benzaldehyde is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

259525-35-4

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259525-35-4 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 259525-35-4 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 2,5,9,5,2 and 5 respectively; the second part has 2 digits, 3 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 259525-35:
(8*2)+(7*5)+(6*9)+(5*5)+(4*2)+(3*5)+(2*3)+(1*5)=164
164 % 10 = 4
So 259525-35-4 is a valid CAS Registry Number.

259525-35-4Relevant academic research and scientific papers

A versatile supported silver for heterogeneously catalysed processes: Synthesis of 3-Acyloxylindolines solvent-free conditions

Sadeghzadeh, Seyed Mohsen,Zhiani, Rahele,Emrani, Shokufe

, (2018)

We have found that fibrous nanosilica (KCC-1) can used as a excellent support for the synthesis of highly sparse nanoparticles and has high surface area that was functionalized with Tetrathia-azacyclopentadecane (TTACP) groups acting as the strong performers so that the Ag nanoparticles were well-dispersed without aggregation on the fibers of the KCC-1 microspheres (KCC-1/TTACP/Ag). We enthusiasm to report one-pot synthesis of 3-Acyloxylindolines for first time from N-tosyl-2-vinylaniline, and benzoic acid in the presence of KCC-1/TTACP/Ag as a catalyst.

The reduction of 4-nitrophenol and 2-nitroaniline by the incorporation of Ni@Pd MNPs into modified UiO-66-NH2 metal-organic frameworks (MOFs) with tetrathia-azacyclopentadecane

Sadeghzadeh, Seyed Mohsen,Zhiani, Rahele,Emrani, Shokufe

, p. 988 - 994 (2018)

We have found that UiO-66-NH2 can be used as an excellent support for the synthesis of highly sparse nanoparticles. UiO-66-NH2 has a high surface area that was functionalized with tetrathia-azacyclopentadecane (TTACP) groups acting as strong conjugation sites so that Ni@Pd nanoparticles were well dispersed without aggregation on the structures of the UiO-66-NH2 microspheres (UiO-66-NH2/TTACP/Ni@Pd). The synthesized UiO-66-NH2/TTACP/Ni@Pd magnetic nanoparticles (MNPs) exhibited excellent catalytic activity for the reduction of 2-nitroaniline and 4-nitrophenol.

A BODIPY-based sensor for Hg2+ in living cells

Zhang, Taiping,She, Guangwei,Qi, Xiaopeng,Mu, Lixuan

supporting information, p. 7102 - 7106 (2013/07/26)

A BODIPY-based probe has been investigated for fast response to Hg 2+ with high sensitivity and selectivity in living cells. This response is attributed to intramolecular charge transfer (ICT) mechanisms. The detection limit is lower than the u

Synthesis and silver ion complexation behavior of fluoroionophores containing a benzothiazolyl group linked to an n-phenylpoly-thiazaalkane moiety

Ishikawa, Junichi,Sakamoto, Hidefumi,Wada, Hiroko

, p. 1273 - 1279 (2007/10/03)

Cyclic and acyclic polythiazaalkane derivatives bearing a benzothiazolyl group as a fluorophore have been synthesized The protonation and the metal ion complexation behavior were studied in a 1,4-dioxane-water (52/48 v/v) solution by spectrophotometry and

Hydrazones Derived from Dithiamonoaza and Tetrathiamonoaza Analogs of Polyethers as Silver Ion Selective Ionophores: Syntheses, Proton-dissociation Behaviors, and Metal Ion Complexing Properties in 1,4-Dioxane-Water Acidic Solution

Ishikawa, Junichi,Sakamoto, Hidefumi,Mizuno, Tamao,Otomo, Makoto

, p. 3071 - 3076 (2007/10/03)

Cyclic and acyclic dithiamonoaza, tetrathiamonoaza, and tetrathiadiaza analogs of polyethers bearing a hydrazone moiety on nitrogen atom(s) were synthesized.Their acidity constants in 1,4-dioxane-water solution and stability constants of hydrazones derive

Silver Selectivity of Novel Monoazapolythioether Derivatives Bearing a Hydrazone Group in the Solvent Extraction

Sakamoto, Hidefumi,Ishikawa, Junichi,Mizuno, Tamao,Doi, Kunio,Otomo, Makoto

, p. 609 - 612 (2007/10/02)

Novel acyclic and cyclic monoazapolythioether derivatives incorporating a substituted hydrazone group were synthesized. The acyclic and cyclic monoazatetrathioether derivatives exhibited high Ag+ ion selectivity in the extraction with 1,2-dichl

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