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Hydrazinecarbothioamide, 2-[(2,5-dihydroxyphenyl)methylene]-, also known as 2-[(2,5-dihydroxyphenyl)methylene]hydrazinecarbothioamide, is a chemical compound with the molecular formula C8H8N2O2S. It is a derivative of hydrazinecarbothioamide, featuring a 2,5-dihydroxyphenyl group attached to the methylene bridge. Hydrazinecarbothioamide, 2-[(2,5-dihydroxyphenyl)methylene]- is characterized by its aromatic ring structure with two hydroxyl groups at the 2nd and 5th positions, which can participate in various chemical reactions due to their reactivity. It is often used in the synthesis of pharmaceuticals and other organic compounds, particularly those involving the formation of complex molecular structures. The compound's properties, such as its solubility and stability, can be influenced by the presence of these functional groups, making it a versatile building block in organic chemistry.

7410-41-5

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7410-41-5 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 7410-41-5 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,4,1 and 0 respectively; the second part has 2 digits, 4 and 1 respectively.
Calculate Digit Verification of CAS Registry Number 7410-41:
(6*7)+(5*4)+(4*1)+(3*0)+(2*4)+(1*1)=75
75 % 10 = 5
So 7410-41-5 is a valid CAS Registry Number.

7410-41-5Downstream Products

7410-41-5Relevant academic research and scientific papers

New thiosemicarbazone Schiff base ligands: Synthesis, characterization, catecholase study and hemolytic activity

Nehar, Oussama Kheireddine,Mahboub, Radia,Louhibi, Samira,Roisnel, Thierry,Aissaoui, Mohammed

, (2020)

Two novel thiosemicarbazones ligands have been synthesized and characterized by FT-IR, ESI-MS, 1H NMR, and also by single-crystal X-ray diffraction for L1. The crystal structure shows that L1 molecules are planar and are connected via N-H----S

Investigation of the salicylaldehyde thiosemicarbazone scaffold for inhibition of influenza virus PA endonuclease

Rogolino, Dominga,Bacchi, Alessia,De Luca, Laura,Rispoli, Gabriele,Sechi, Mario,Stevaert, Annelies,Naesens, Lieve,Carcelli, Mauro

, p. 1109 - 1121 (2015/10/19)

The influenza virus PA endonuclease is an attractive target for the development of novel anti-influenza virus therapeutics, which are urgently needed because of the emergence of drug-resistant viral strains. Reported PA inhibitors are assumed to chelate t

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