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65562-34-7

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  • [3,4,5-triacetyloxy-6-[(5Z)-5-[(5-bromothiophen-2-yl)methylidene]-4-oxo-2-sulfanylidene-thiazolidin-3-yl]oxan-2-yl]methyl acetate

    Cas No: 65562-34-7

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  • [3,4,5-triacetyloxy-6-[(5Z)-5-[(5-bromothiophen-2-yl)methylidene]-4-oxo-2-sulfanylidene-thiazolidin-3-yl]oxan-2-yl]methyl acetate cas 65562-34-7

    Cas No: 65562-34-7

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65562-34-7 Usage

General Description

The chemical "(5Z)-5-[(5-bromothiophen-2-yl)methylidene]-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one" is a compound that contains a thiazolidin-4-one ring and a bromothiophene group. It also has acetylhexopyranosyl groups attached. (5Z)-5-[(5-bromothiophen-2-yl)methylidene]-3-(2,3,4,6-tetra-O-acetylhexopyranosyl)-2-thioxo-1,3-thiazolidin-4-one has potential biological activity and may be of interest for medicinal or pharmaceutical purposes. The specific properties and potential applications of this compound would need to be further evaluated through research and experimentation.

Check Digit Verification of cas no

The CAS Registry Mumber 65562-34-7 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, 3 and 4 respectively.
Calculate Digit Verification of CAS Registry Number 65562-34:
(7*6)+(6*5)+(5*5)+(4*6)+(3*2)+(2*3)+(1*4)=137
137 % 10 = 7
So 65562-34-7 is a valid CAS Registry Number.

65562-34-7SDS

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-[(5Z)-5-[(5-bromothiophen-2-yl)methylidene]-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

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More Details:65562-34-7 SDS

65562-34-7Downstream Products

65562-34-7Relevant 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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