34709-44-9

Basic information

• Product Name: 5-[(2-hydroxyphenyl)methylidene]-2-thioxo-1,3-thiazolidin-4-one
• CAS NO: 34709-44-9
• Molecular Formula: C₁₀H₇NO₂S₂
• Molecular Weight: 237.2981
• Mol File: 34709-44-9.mol
• Article Data: 7

Chemical Properties

• Density: 1.56g/cm³
• Refractive Index: 1.776
• CAS DataBase Reference: 5-[(2-hydroxyphenyl)methylidene]-2-thioxo-1,3-thiazolidin-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: 5-[(2-hydroxyphenyl)methylidene]-2-thioxo-1,3-thiazolidin-4-one(34709-44-9)
• EPA Substance Registry System: 5-[(2-hydroxyphenyl)methylidene]-2-thioxo-1,3-thiazolidin-4-one(34709-44-9)

Safety Data

• Hazardous Substances Data: 34709-44-9(Hazardous Substances Data)

Usage

Description

5-[(2-hydroxyphenyl)methylidene]-2-thioxo-1,3-thiazolidin-4-one is a complex chemical compound characterized by a thiazolidin-4-one ring with a thioxo group and a methylidene group. It also features a hydroxyphenyl group attached to the carbon atom, which imparts unique properties to the molecule. This versatile chemical is known for its potential applications in pharmaceuticals, organic synthesis, and as a building block for synthesizing other complex organic compounds.

Uses

Used in Pharmaceutical Industry:
5-[(2-hydroxyphenyl)methylidene]-2-thioxo-1,3-thiazolidin-4-one is used as a pharmaceutical compound for its potential therapeutic properties. Its unique structure and reactivity make it a promising candidate for the development of new drugs and treatments.
Used in Organic Synthesis:
In the field of organic synthesis, 5-[(2-hydroxyphenyl)methylidene]-2-thioxo-1,3-thiazolidin-4-one serves as a key intermediate or building block. It can be utilized in the synthesis of a variety of complex organic compounds, contributing to the advancement of chemical research and development.
Used in Material Science:
5-[(2-hydroxyphenyl)methylidene]-2-thioxo-1,3-thiazolidin-4-one is also used in material science for its potential applications in creating new materials with unique properties. Its versatility allows it to be incorporated into various materials, enhancing their performance and functionality.

Upstream product

• 141-84-4 2-thioxo-4-thiazolidinone 
• 90-02-8 salicylaldehyde 
• 89-95-2 2-methyl-benzyl alcohol 

Downstream Products

• 852311-72-9 4-Hydrazono-5-[1-(2-hydroxy-phenyl)-meth-(E)-ylidene]-thiazolidine-2-thione 
• 81154-06-5 E-5-(2-hydroxyphenylmethylene)-2-morpholino-4-oxo-2-thiazoline 

Relevant articles and documents

Synthesis and applications of some new nitrogen-containing heterocyclic azo-disperse dyes bearing quinoline chromophore

A set of five novel nitrogen-containing heterocyclic azo-disperse dyes 8 (a–d) and 10 were synthesized by diazotization of 4-bisaminoquinolines 3, followed by coupling either with rhodanine analogues 6 modified at C-5 position or α-naphthol 9. The chemica

Synthesis, structure analysis, investigation of conductivity, thermal properties of polyphenol derivatives containing a rhodanine moiety and their Cu(II), VO(IV) complexes

In this study, 5-benzylidenerhodanine derivatives namely 5-(2-hydroxybenzylidene)-2-thioxothiazolidin-4-one (SAR) and 5-((2-hydroxynaphthalen-1-yl)methylene)-2-thioxothiazolidin-4-one (HNAR) used as monomer. The new polymers of SAR and HNAR (PSAR and PHNA

A solvent-free protocol for the green synthesis of arylalkylidene rhodanines in a task-specific ionic liquid

2-Hydroxyethylammonium formate acts as a task-specific ionic liquid (TSIL) for the Knoevenagel condensation of carbonyl compounds with rhodanine to afford arylalkylidene rhodanines under solvent-free conditions and in good-to-excellent yields. Additionally, compared with those in organic solvents, the yields obtained in the presence of our ionic liquid (IL) were significantly increased. The detailed mechanism of the catalytic effect of TSIL is also reported for the first time.