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2,6-diacetylpyridine bis-4-phenyl-3-thiosemicarbazone is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

134293-68-8

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134293-68-8 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 134293-68-8 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 1,3,4,2,9 and 3 respectively; the second part has 2 digits, 6 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 134293-68:
(8*1)+(7*3)+(6*4)+(5*2)+(4*9)+(3*3)+(2*6)+(1*8)=128
128 % 10 = 8
So 134293-68-8 is a valid CAS Registry Number.

134293-68-8Downstream Products

134293-68-8Relevant academic research and scientific papers

Analytical applications of 2,6-diacetylpyridine-bis-4-phenyl-3-thiosemicarbazone (2,6-DAPBPTSC): Determination of cd(II) in foods and water samples

Adinarayana Reddy,Janardhan Reddy,Varada Reddy

, p. 236 - 243 (2010)

To the determination of trace amount of Cd(II) present in food and water samples, a selective and extractive spectrophotometric method were developed with 2,6-diacetylpyridine-bis-4-phenyl-3-thiosemi-carbazone as a complexing agent. The yellowish orange c

Synthesis of a series of novel In(iii) 2,6-diacetylpyridine bis(thiosemicarbazide) complexes: Structure, anticancer function and mechanism

Li, Shanhe,Khan, Muhammad Hamid,Wang, Xiaojun,Cai, Meiling,Zhang, Juzheng,Jiang, Ming,Zhang, Zhenlei,Wen, Xiao-An,Liang, Hong,Yang, Feng

, p. 17207 - 17220 (2020)

The anticancer function and anticancer mechanism of indium (In) complexes still remain mysterious to date. Furthermore, it is greatly challenging to design a multi-functional metal agent that not only kills cancer cells but also inhibits their invasion an

Complexes of Cu(II) and Ni(II) with bis(phenylthiosemicarbazone): Synthesis, spectral, EPR and in vitro - Antibacterial and antioxidant activity

Rao, Y. Subba,Prathima,Reddy, S. Adinarayana,Madhavi,Reddy, A. Varada

, p. 677 - 682 (2010)

The synthesis of Cu(II) and Ni(II) complexes with 2,6-diacetylpyridine bis(4-phenyl-3-thiosemicarbazone) (L) ligand have been reported. The ligand was characterized by elemental analysis and spectral (IR and 1H NMR) studies and its complexes were characte

The Effect of Substituents on Catalytic Performance of bis-Thiosemicarbazone Mo(VI) Complexes: Synthesis and Spectroscopic, Electrochemical, and Functional Properties

Moradi-Shoeili,Zare

, p. 203 - 210 (2018)

The preparation, characterization and electrochemical properties are reported for three new types of molybdenum(VI) complexes with bis-thiosemicarbazone ligands. All compounds were characterized by elemental analysis, electronic spectra, IR and 1/su

Cytotoxic activity of expanded coordination bis-thiosemicarbazones and copper complexes thereof

Akladios, Fady N.,Andrew, Scott D.,Parkinson, Christopher J.

, p. 931 - 944 (2016)

A series of bis-thiosemicarbazone agents with coordinating groups capable of multiple metal coordination modes has been generated and evaluated for potential cytotoxic effects against melanoma (MelRm) and breast adenocarcinoma (MCF-7) cell lines. The bis-

Indium compound with 2,6-diacetylpyridine thiosemicarbazone as ligand and synthesis method and application of indium compound

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Paragraph 0042-0045, (2019/04/30)

The invention discloses an indium compound with 2,6-diacetylpyridine thiosemicarbazone as a ligand and a synthesis method and application of the indium compound. The synthesis method includes the following steps that 2,6-diacetylpyridine is dissolved in e

In order to 2, 6 - diacetyl pyridine thiosemicarbazone ligand zinc compound and its synthetic method and application (by machine translation)

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Paragraph 0030, (2018/04/02)

The invention discloses a method for 2, 6 - diacetyl pyridine thiosemicarbazone ligand zinc compound and its synthetic method and application, the zinc compound is synthetic six to 2, 6 - diacetyl pyridine thiosemicarbazone as ligand complex Zn, and the z

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