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

Description

(5Z)-5-[4-(dimethylamino)phenyl]methylidene-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one is a complex organic molecule with a unique structure that features a thiazolidin-4-one ring, a thioxo group, a hexopyranosyl ring with four acetyl groups, a phenyl group with a dimethylamino substituent, and a methylidene group. Its intricate composition suggests potential applications in medicinal chemistry, particularly as a candidate for therapeutic purposes. Further research is necessary to explore its properties and uses.

Uses

Used in Pharmaceutical Industry:
(5Z)-5-[4-(dimethylamino)phenyl]methylidene-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one is used as a potential drug candidate for various therapeutic applications due to its complex molecular structure and the presence of multiple functional groups that may interact with biological targets.
Used in Medicinal Chemistry Research:
In the field of medicinal chemistry, this compound is used as a subject of study to understand its interactions with biological systems. (5Z)-5-[4-(dimethylamino)phenyl]methylidene-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one's unique structure may provide insights into new mechanisms of action or reveal novel pharmacological properties that could be harnessed for the development of new drugs.

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.