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Hydrazinecarbothioamide, 2-[(2-hydroxy-3-methoxyphenyl)methylene]- is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

51146-75-9

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51146-75-9 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 51146-75-9 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 5,1,1,4 and 6 respectively; the second part has 2 digits, 7 and 5 respectively.
Calculate Digit Verification of CAS Registry Number 51146-75:
(7*5)+(6*1)+(5*1)+(4*4)+(3*6)+(2*7)+(1*5)=99
99 % 10 = 9
So 51146-75-9 is a valid CAS Registry Number.

51146-75-9 Well-known Company Product Price

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  • (18894)  2-Hydroxy-3-methoxybenzaldehyde thiosemicarbazone  for spectrophotometric determination of Ni2+, ≥99.0% (HPLC)

  • 51146-75-9

  • 18894-10G

  • 3,492.45CNY

  • Detail

51146-75-9SDS

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 [(5-methoxy-6-oxocyclohexa-2,4-dien-1-ylidene)methylamino]thiourea

1.2 Other means of identification

Product number -
Other names o-vanillin thiosemicarbazone

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:51146-75-9 SDS

51146-75-9Relevant academic research and scientific papers

Synthesis, spectroscopic and single crystal X-ray studies on three new mononuclear Ni(II) pincer type complexes: DFT calculations and their antimicrobial activities

Layek, Samaresh,Agrahari, Bhumika,Tarafdar, Abhrajyoti,Kumari, Chanda,Anuradha,Ganguly, Rakesh,Pathak, Devendra D.

, p. 428 - 435 (2017)

Three new mononuclear square planar Ni(II) complexes, containing pincer type tridentate Schiff base ligands, having general formula [(NiL1(4-MePy)] (1), [(NiL1(2-AzNp)] (2), and [(NiL2(4-MePy)] (3) [where L1?=?a

Synthesis, spectroscopic characterization, structural studies and antibacterial and antitumor activities of diorganotin complexes with 3-methoxysalicylaldehyde thiosemicarbazone

Khandani, Marzieh,Sedaghat, Tahereh,Erfani, Nasrollah,Haghshenas, Mohammad Reza,Khavasi, Hamid Reza

, p. 136 - 143 (2013)

Three organotin(IV) complexes, Ph2Sn(mstsc) (1), Me 2Sn(mstsc) (2) and Bu2Sn(mstsc) (3), have been synthesized from reaction of R2SnCl2 (R = Ph, Me and Bu) with 3-methoxysalicylaldehyde thiosemicarbaz

Synthesis and characterization of thiazole and 2-thioxoimidazolidinone derivative; Their antibacterial and anticancer properties

Sherif, Mohamed H.,Eldeen, Ibrahim M.,Helal, Eman O.

, p. 3949 - 3968 (2013)

5-Aryl-2-[(5-substituted-3-methoxy-2-hydroxybenzylidene)-hydrazine] -thiazoles (3a,b) and 3-[(5-substituted-3-methoxy-2-hydroxybenzylidene)amino]-4- oxo-imidazolidin-2-thiones (4a,b) were prepared via cyclization of 5-substituted-3-methoxy-2-hydroxy-benza

Antiproliferative activity of nickel(II), palladium(II) and zinc(II) thiosemicarbazone complexes

Buschini, A.,Carcelli, M.,Gandin, V.,Miglioli, F.,Montalbano, S.,Pelosi, G.,Rogolino, D.

supporting information, (2022/01/13)

Complexes of nickel(II), palladium(II) and zinc(II) have been synthesized with four ONS thiosemicarbazone tridentate ligands. The ligands were obtained from the synthesis of 2-hydroxy-3-methoxybenzaldehyde or 2,3-dihydroxybenzaldehyde with thiosemicarbazi

Fluorescent Cu(II) complex as chemosensor for the detection of L-Aspartic acid with high selectivity and sensitivity

Dallemer, F.,Kalaivani, P.,Kalpana, T.,Prabhakaran, R.,Ranjani, M.,Selvakumar, S.

supporting information, (2021/11/17)

3-methoxysalicylaldehyde thiosemicarbazone (PL) was used as chemosensor for the detection of various cations (chloride salts). Among them, Cu2+ and Hg2+ ions showed drastic decrease in their fluorescence intensity and colorimetric ti

Gold complex taking o-vanillin thiosemicarbazone as ligand and synthesis method thereof

-

Paragraph 0010; 0026-0029, (2021/01/29)

The invention discloses a gold complex taking o-vanillin thiosemicarbazone as a ligand and a synthesis method thereof. During synthesis, thiosemicarbazone is dissolved in methanol, o-vanillin is added, reflux reaction and filtration are performed, filtrat

SOLVENT FREE SYNTHESIS of HYDRAZINE CARBOTHIOAMIDE DERIVATIVES AS A PRECURSOR in the PREPARATION of NEW MONONUCLEAR Mn(II), Cu(II), and Zn(II) COMPLEXES: SPECTROSCOPIC CHARACTERIZATIONS

Al-Hazmi, Ghaferah H.,Alosaimi, Abeer M.,Refat, Moamen S.,Saad, Hosam A.

, p. 413 - 424 (2022/01/03)

Over the last few years considerable attention has been devoted to the study of Schiff base complexes of metal(II) containing nitrogen, oxygen and sulfur donor ligands due to their diverse biological activities. Therefore, the Schiff base thiosemicarbazon

Organoruthenium(II) complexes attenuate stress in Caenorhabditis elegans through regulating antioxidant machinery

Mohankumar,Devagi,Shanmugam,Nivitha,Sundararaj,Dallemer,Kalaivani,Prabhakaran

supporting information, p. 123 - 133 (2019/02/26)

The 1:1 stoichiometric reactions of 3-methoxy salicylaldehyde-4(N)-substituted thiosemicarbazones (H2L1?4) with [RuCpCl(PPh3)2] was carried out in methanol. The obtained complexes (1–4) were characterized by ana

Benzaldehyde thiosemicarbazone derivatives against replicating and nonreplicating Mycobacterium tuberculosis

Volynets, Galyna P.,Tukalo, Michail A.,Bdzhola, Volodymyr G.,Derkach, Nataliia M.,Gumeniuk, Mykola I.,Tarnavskiy, Sergiy S.,Starosyla, Sergiy A.,Yarmoluk, Sergiy M.

, p. 218 - 224 (2019/01/29)

In this article, we report a series of benzaldehyde thiosemicarbazone derivatives possessing high activity toward actively replicating Mycobacterium tuberculosis strain with minimum inhibitory concentration (MIC) values in the range from 0.14 to 2.2 μM. Among them, two compounds—2-(4-phenethoxybenzylidene)hydrazine-1-carbothioamide (13) and 2-(3-isopropoxybenzylidene)hydrazine-1-carbothioamide (20) also demonstrate submicromolar antimycobacterial activity against M. tuberculosis under hypoxia with MIC values of 0.68 and 0.74 μM, respectively. The activity of compounds 13 and 20 toward five investigated isoniazid-, rifampicin-, and fluoroquinolone-resistant M. tuberculosis isolates is similar to commercially available antituberculosis drugs. The compounds 13 and 20 possess good ADME properties and have low cytotoxicity toward human liver cells (HepG2). Therefore, 2-(4-phenethoxybenzylidene)hydrazine-1-carbothioamide (13) and 2-(3-isopropoxybenzylidene)hydrazine-1-carbothioamide (20) are valuable candidates for further preclinical studies.

Half-Sandwich Arene Ruthenium(II) and Osmium(II) Thiosemicarbazone Complexes: Solution Behavior and Antiproliferative Activity

Gatti, Anna,Habtemariam, Abraha,Romero-Canelón, Isolda,Song, Ji-Inn,Heer, Bindy,Clarkson, Guy J.,Rogolino, Dominga,Sadler, Peter J.,Carcelli, Mauro

, p. 891 - 899 (2018/03/30)

We report the synthesis, characterization, and antiproliferative activity of organo-osmium(II) and organo-ruthenium(II) half-sandwich complexes [(η6-p-cym)Os(L)Cl]Cl (1 and 2) and [(η6-p-cym)Ru(L)Cl]Cl (3 and 4), where L = N-(2-hydro

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