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65562-30-3

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  • [3,4,5-triacetyloxy-6-[(5E)-5-[1-(2-furyl)ethylidene]-4-oxo-2-sulfanylidene-thiazolidin-3-yl]oxan-2-yl]methyl acetate

    Cas No: 65562-30-3

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  • [3,4,5-triacetyloxy-6-[(5E)-5-[1-(2-furyl)ethylidene]-4-oxo-2-sulfanylidene-thiazolidin-3-yl]oxan-2-yl]methyl acetate cas 65562-30-3

    Cas No: 65562-30-3

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65562-30-3 Usage

General Description

The chemical compound "(5E)-5-(1-furan-2-ylethylidene)-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one" is a complex molecule containing a thiazolidin-4-one ring, a furan-2-ylethylidene group, and an O-acetylhexopyranosyl moiety. It is characterized by its thioxo and thiazolidin functionalities, which are important for potential biological and pharmacological activities. The compound's acetylhexopyranosyl group suggests that it may have potential as a glycoside or carbohydrate derivative, possibly with implications for its solubility or cellular uptake. The overall structure and functionalities present in this compound make it a candidate for further investigation in the fields of medicinal chemistry and drug development.

Check Digit Verification of cas no

The CAS Registry Mumber 65562-30-3 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, 3 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 65562-30:
(7*6)+(6*5)+(5*5)+(4*6)+(3*2)+(2*3)+(1*0)=133
133 % 10 = 3
So 65562-30-3 is a valid CAS Registry Number.

65562-30-3SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 13, 2017

Revision Date: Aug 13, 2017

1.Identification

1.1 GHS Product identifier

Product name [3,4,5-triacetyloxy-6-[(5E)-5-[1-(furan-2-yl)ethylidene]-4-oxo-2-sulfanylidene-1,3-thiazolidin-3-yl]oxan-2-yl]methyl acetate

1.2 Other means of identification

Product number -
Other names -

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

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More Details:65562-30-3 SDS

65562-30-3Relevant articles and documents

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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