59157-24-3

Usage

Appearance

Yellow solid
The compound has a yellow color and is in a solid state at room temperature.

Solubility

Soluble in organic solvents
The compound can dissolve in certain organic solvents, such as ethanol, acetone, or dichloromethane.

Chemical classification

Hydrazinecarbothioamide derivative
The compound belongs to a class of chemical compounds known as hydrazinecarbothioamides.

Structural features

Substituted naphthalene ring and a phenyl group
The compound has a naphthalene ring with a substituent (2-oxo) and a phenyl group attached to the main structure.

Biological activity

Potential in medicinal chemistry
The compound has shown potential for biological activity, particularly in the field of medicinal chemistry, making it a subject of interest for research and development.

Applications

Possible use in various fields of study
Due to its specific properties and potential applications, the compound may warrant further investigation in different areas of study, such as pharmaceuticals, agrochemicals, or materials science.

Upstream product

• 5351-69-9 4-Phenyl-3-thiosemicarbazide 
• 708-06-5 2-hydroxynaphthalene-1-carbaldehyde 

Downstream Products

• 1261244-85-2 [RuCl₂(dimethyl sulfoxide)2(2-hydroxy-1-naphthaldehyde 4-phenylthiosemicarbazone)] 

Relevant academic research and scientific papers

2-Hydroxy-naphth-1-aldehyde phenyl-thiosemicarbazone: Effective thiourea-based sensor for acetate anion

A novel urea-based sensor displaying selective recognition for AcO - had been designed and synthesized. Experiments showed that sensor 1 can selectively recognize acetate in DMSO. The evaluation of the sensor's interaction with a variety of structurally different anions was performed by UV-vis titration experiments in DMSO. In addition, the nature of interaction between sensor 1 and AcO- was investigated by 1H NMR titrations.

A new use for an old molecule: N-phenyl-2-(2-hydroxynaphthalen-1- ylmethylene)hydrazinecarbothioamide as a ratiometric 'Off-On' fluorescent probe for iron

N-Phenyl-2-(2-hydroxynaphthalen-1-ylmethylene)hydrazinecarbothioamide has been investigated as a fluorescent sensor for the determination of Fe(III) in aqueous solutions. The probe was prepared by the facile Schiff base condensation of 2-hydroxy-1-napthal

In vitro antiproliferative activity of palladium(ii) thiosemicarbazone complexes and the corresponding functionalized chitosan coated magnetite nanoparticles

This work reports the synthesis and characterization of palladium(ii) complexes Pd(L1)2 (1), Pd(L2)2 (2), Pd(L3)2 (3) and Pd(L4)2 (4), where L1H: 1-naphthal

Developing anticancer ferric prodrugs based on the N-donor residues of human serum albumin carrier IIA subdomain

To improve the selectivity, delivery, and activity of ferric (Fe) anticancer agents, we design prodrugs based on N-donor residues of the human serum albumin (HSA) carrier IIA subdomain. We synthesized six Fe(III) compounds derived from 2-hydroxy-1-naphtha

Diorganotin Complexes with N(4)-Phenylthiosemicarbazones: Synthesis, Spectroscopic Characterization, and Antibacterial Activity

The organotin(IV) complexes, SnPh2La (1), SnMe 2La (2), SnBu2La (3), SnPh 2Lb (4), SnMe2Lb (5), SnPh 2Lc (6), SnMe2/s