51859-60-0

Basic information

• Product Name: 2-FURAN-2-YL-THIAZOLIDINE
• Synonyms: 2-FURAN-2-YL-THIAZOLIDINE;2-(2-FURYL)-1,3-THIAZOLIDINE;2-(2-FURYL)THIAZOLIDINE;2-(furan-2-yl)-1,3-thiazolidine
• CAS NO: 51859-60-0
• Molecular Formula: C7H9NOS
• Molecular Weight: 155.22
• Mol File: 51859-60-0.mol
• Article Data: 2

Chemical Properties

• Melting Point: 54-55 °C
• Boiling Point: 277.9°Cat760mmHg
• Flash Point: 121.9°C
• Appearance: /
• Density: 1.183g/cm³
• Vapor Pressure: 0.00441mmHg at 25°C
• Refractive Index: 1.554
• PKA: 7.74±0.40(Predicted)
• CAS DataBase Reference: 2-FURAN-2-YL-THIAZOLIDINE(CAS DataBase Reference)
• NIST Chemistry Reference: 2-FURAN-2-YL-THIAZOLIDINE(51859-60-0)
• EPA Substance Registry System: 2-FURAN-2-YL-THIAZOLIDINE(51859-60-0)

Safety Data

• Hazard Codes: Xi
• HazardClass: IRRITANT
• Hazardous Substances Data: 51859-60-0(Hazardous Substances Data)

Usage

General Description

2-FURAN-2-YL-THIAZOLIDINE is a chemical compound that consists of a thiazolidine ring with a furan group attached to it. It is often used in pharmaceutical research and drug development due to its potential biological activities. Thiazolidine derivatives have been studied for their anti-inflammatory, antioxidant, and anti-cancer properties. The furan group in 2-FURAN-2-YL-THIAZOLIDINE may contribute to its bioactivity, as furan-containing compounds have been found to exhibit various pharmacological effects. Overall, 2-FURAN-2-YL-THIAZOLIDINE shows promise as a potential lead compound for the development of new pharmaceutical agents.

InChI:InChI=1/C7H9NOS/c1-2-6(9-4-1)7-8-3-5-10-7/h1-2,4,7-8H,3,5H2

Upstream product

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Relevant articles and documents

Structured fluids as microreactors for flavor formation by the maillard reaction

Thermal reactions of cysteine/furfural and cysteine/ribose mixtures were studied in model systems to gain more insight into the influence of structured fluids such as L2 microemulsions and cubic phases on the generation of aroma compounds. Formation of 2-furfurylthiol from cysteine/furfural was particularly efficient in L2 microemulsions and cubic phases compared to aqueous systems. The reaction led to the formation of two new sulfur compounds, which were identified as 2-(2-furyl)thiazolidine and, tentatively, N-(2-mercaptovinyl)-2-(2-furyl)thiazolidine. Similarly, generation of 2-furfurylthiol and 2-methyl-3-furanthiol from cysteine/ribose mixtures was strongly enhanced in structured fluids. The cubic phase was shown to be even more efficient in flavor generation than the L2 microemulsion. It was denoted 'cubic catalyst' or 'cubic selective microreactor'. The obtained results are interpreted in terms of a surface and curvature control of the reactions defined by the structural properties of the formed surfactant associates.