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(5Z)-5-[(2,6-dichlorophenyl)methylidene]-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one is a complex organic compound characterized by a thiazolidinone ring, which is a five-membered heterocyclic ring containing both sulfur and nitrogen atoms. It also features a benzene ring with two chlorine atoms and multiple acetyl groups attached to a hexopyranosyl unit. This diverse chemical structure may endow it with potential applications in various fields, such as pharmaceuticals or materials science.

65562-26-7

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65562-26-7 Usage

Uses

Used in Pharmaceutical Industry:
(5Z)-5-[(2,6-dichlorophenyl)methylidene]-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one is used as a pharmaceutical compound for its potential therapeutic properties. The presence of the thiazolidinone ring and the chlorine-substituted benzene ring may contribute to its biological activity, making it a candidate for the development of new drugs.
Used in Materials Science:
In the field of materials science, (5Z)-5-[(2,6-dichlorophenyl)methylidene]-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one may be utilized for the development of novel materials with unique properties. The combination of different functional groups in its structure could lead to the creation of materials with specific characteristics, such as improved stability or reactivity.

Check Digit Verification of cas no

The CAS Registry Mumber 65562-26-7 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 6,5,5,6 and 2 respectively; the second part has 2 digits, 2 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 65562-26:
(7*6)+(6*5)+(5*5)+(4*6)+(3*2)+(2*2)+(1*6)=137
137 % 10 = 7
So 65562-26-7 is a valid CAS Registry Number.

65562-26-7Downstream Products

65562-26-7Relevant academic research and scientific papers

N glucopyranosyl 5 aralkylidenerhodanines: Synthesis and antibacterial and antiviral activities

Foye,Tovivich

, p. 1607 - 1611 (2007/10/08)

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.

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