65562-39-2

Basic information

• Product Name: (5E)-5-(1-pyridin-4-ylethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one
• CAS NO: 65562-39-2
• Molecular Formula: C₂₄H₂₆N₂O₁₀S₂
• Molecular Weight: 566.6006
• Mol File: 65562-39-2.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 643.5°C at 760 mmHg
• Flash Point: 343°C
• Density: 1.44g/cm³
• Vapor Pressure: 1.89E-16mmHg at 25°C
• Refractive Index: 1.613
• CAS DataBase Reference: (5E)-5-(1-pyridin-4-ylethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: (5E)-5-(1-pyridin-4-ylethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one(65562-39-2)
• EPA Substance Registry System: (5E)-5-(1-pyridin-4-ylethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one(65562-39-2)

Safety Data

• Hazardous Substances Data: 65562-39-2(Hazardous Substances Data)

Usage

General Description

The chemical "(5E)-5-(1-pyridin-4-ylethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one" is a complex compound containing a thiazolidin-4-one ring, a pyridin-4-ylethylidene group, and a tetra-O-acetylhexopyranosyl group. The thiazolidin-4-one ring contains a thioxo group and a double bond, while the pyridin-4-ylethylidene group is attached to the ring structure. The tetra-O-acetylhexopyranosyl group is a sugar molecule with four acetyl groups attached to a hexopyranosyl ring. (5E)-5-(1-pyridin-4-ylethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one likely has biological activity and may be used in medicinal chemistry research due to its complex structure and potential interaction with biological systems.

Upstream product

• 572-09-8 2,3,4,6-tetra-O-acetyl-α-D-glucopyranosyl bromide 

Relevant articles and documents

N glucopyranosyl 5 aralkylidenerhodanines: Synthesis and antibacterial and antiviral activities

A series of N-(2,3,4,6-tetra-O-acetyl-β-D-glucopyranosyl)-5-aralkylidenerhodanines was synthesized, and the acetyl groups were removed to give N-β-D-glucopyranosyl-5-aralkylidenerhodanines without cleavage of the rhodanine ring by means of acid hydrolysis. Alkaline hydrolysis with ammonia in methanol resulted in cleavage to N-glucosylthiourea, providing evidence for N-glycoside formation. A number of the rhodanine derivatives, especially those with nitro or chloro groups in the aromatic ring, showed antibacterial activity. N-β-D-Glucopyranosyl-5-(4-nitrobenzylidene)rhodanine showed antiviral activity by inhibition of viral RNA synthesis. Some effect on blood sugar levels also was observed with several rhodanines.