65562-21-2

Basic information

• Product Name: (5Z)-5-{[4-(dimethylamino)phenyl]methylidene}-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one
• CAS NO: 65562-21-2
• Molecular Formula: C₂₆H₃₀N₂O₁₀S₂
• Molecular Weight: 594.6538
• Mol File: 65562-21-2.mol
• Article Data: 1

Chemical Properties

• Boiling Point: 670.8°C at 760 mmHg
• Flash Point: 359.5°C
• Density: 1.41g/cm³
• Vapor Pressure: 7.37E-18mmHg at 25°C
• Refractive Index: 1.617
• CAS DataBase Reference: (5Z)-5-{[4-(dimethylamino)phenyl]methylidene}-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one(CAS DataBase Reference)
• NIST Chemistry Reference: (5Z)-5-{[4-(dimethylamino)phenyl]methylidene}-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one(65562-21-2)
• EPA Substance Registry System: (5Z)-5-{[4-(dimethylamino)phenyl]methylidene}-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one(65562-21-2)

Safety Data

• Hazardous Substances Data: 65562-21-2(Hazardous Substances Data)

Usage

General Description

This chemical compound, with the IUPAC name (5Z)-5-{[4-(dimethylamino)phenyl]methylidene}-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one, is a complex molecule consisting of various functional groups. It contains a thiazolidin-4-one ring, a thioxo group, and a hexopyranosyl ring with four acetyl groups. The compound also features a phenyl group with a dimethylamino substituent and a methylidene group. Due to its intricate structure, this compound may have potential applications in medicinal chemistry, particularly as a potential drug candidate for various therapeutic purposes. However, further studies and research are required to fully understand its properties and potential uses.

Upstream product

• 536-17-4 5-(4-dimethylaminobenzylidene)rhodanine 
• 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.