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The chemical compound "(3alpha,5beta,8xi,9xi,12beta)-12,14-dihydroxy-3-[(2,3,4,6-tetra-O-acetyl-beta-D-glycero-hexopyranosyl)oxy]card-20(22)-enolide" is a complex, naturally occurring lactone with a unique molecular structure. It is characterized by the presence of two hydroxyl groups at the 12th and 14th carbon positions, and a glycosidic linkage at the 3rd position with a tetra-O-acetyl-beta-D-glycero-hexopyranosyl moiety. (3alpha,5beta,8xi,9xi,12beta)-12,14-dihydroxy-3-[(2,3,4,6-tetra-O-acetyl-beta-D-glycero-hexopyranosyl)oxy]card-20(22)-enolide belongs to the cardenolide class, which are known for their cardiotonic properties and are often found in plants of the Apocynaceae family. The specific stereochemistry at various carbon positions, as indicated by the alpha and beta prefixes, is crucial for its biological activity and interaction with target receptors. (3alpha,5beta,8xi,9xi,12beta)-12,14-dihydroxy-3-[(2,3,4,6-tetra-O-acetyl-beta-D-glycero-hexopyranosyl)oxy]card-20(22)-enolide's structure and properties make it a subject of interest in pharmaceutical research, particularly for its potential applications in the treatment of heart conditions.

79317-29-6

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79317-29-6 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 79317-29-6 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 7,9,3,1 and 7 respectively; the second part has 2 digits, 2 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 79317-29:
(7*7)+(6*9)+(5*3)+(4*1)+(3*7)+(2*2)+(1*9)=156
156 % 10 = 6
So 79317-29-6 is a valid CAS Registry Number.

79317-29-6SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name [(3R,6R)-3,4,5-triacetyloxy-6-[[(3S,5R,10S,12R,13S,14S,17R)-12,14-dihydroxy-10,13-dimethyl-17-(5-oxo-2H-furan-3-yl)-1,2,3,4,5,6,7,8,9,11,12,15,16,17-tetradecahydrocyclopenta[a]phenanthren-3-yl]oxy]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:79317-29-6 SDS

79317-29-6Downstream Products

79317-29-6Relevant academic research and scientific papers

Cardenolide analogues. 11. Improved method for the use of Fetizon's reagent in the synthesis of cardiac glycosides

Brown,Boutagy,Thomas

, p. 1059 - 1064 (2007/10/02)

An improved procedure has been developed for preparing glycosides of cardenolide genins. The method uses specially prepared Fetizon's reagent as catalyst, combined, in most cases, with mercuric cyanide and mercuric bromide. In the presence of this catalyst, genins react readily, at room temperature, with per-acetylated 1-bromo-sugars to give the acetylated glycosides in high yield with little or no side reaction. The reaction proceeds almost to completion in 30 to 60 min. The free glycoside is obtained by mild deacetylation using triethylamine/methanol/water (20:20:1) at room temperature for 72 h. Proof of structure was obtained using chemical ionization mass spectrometry, NMR spectroscopy and comparison of physical constants with published data. The compounds were tested for inotropic activity using the isolated guinea pig atrium.

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