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(3beta,5beta,8xi,9xi,16beta)-3,16-bis(formyloxy)-14-hydroxycard-20(22)-enolide is a complex organic compound with a unique molecular structure. It is a derivative of cardenolides, which are a class of steroidal compounds found in plants, particularly in the foxglove family. This specific compound is characterized by the presence of two formyloxy groups at the 3 and 16 positions, a hydroxyl group at the 14 position, and a double bond between the 20 and 22 positions. The compound's structure is further defined by the stereochemistry at the 3, 5, 8, 9, and 16 positions, with beta and xi configurations. This chemical is of interest in the field of natural products chemistry and may have potential applications in pharmaceutical research due to its structural similarity to cardioactive steroids.

1256-58-2

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1256-58-2 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 1256-58-2 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 1,2,5 and 6 respectively; the second part has 2 digits, 5 and 8 respectively.
Calculate Digit Verification of CAS Registry Number 1256-58:
(6*1)+(5*2)+(4*5)+(3*6)+(2*5)+(1*8)=72
72 % 10 = 2
So 1256-58-2 is a valid CAS Registry Number.

1256-58-2SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name [16-formyloxy-14-hydroxy-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] formate

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:1256-58-2 SDS

1256-58-2Downstream Products

1256-58-2Relevant academic research and scientific papers

Cardiac Glycosides. 6. Gitoxigenin C16 Acetates, Formates, Methoxycarbonates, and Digitoxosides. Synthesis and Na+, K+ -ATPase Inhibitory Activities

Hashimoto, Toshihiro,Rathore, Hargovind,Satoh, Daisuke,Hong, George,Griffin, Jane F.,et al.

, p. 997 - 1003 (2007/10/02)

A series of 17 gitoxigenin 16β-formates, acetates, and methoxycarbonates was synthesized, including their 3β-acetates, formates, and digitoxosides.A 16β-formate group was generally found to increase activity 30 times, a 16β-acetate group 9-12 times, while a 16β-methoxycarbonate decreased activity by two-thirds. 3β-Formates and acetates had little effect on activity by themselves, but sometimes reduced the activity-increasing properties of 16β-formates and acetates.A 3β-digitoxoside increases the activity of ditoxigenin by 15 times, but the effect is less ifthe 16β-group is esterified.And finally, a 16-one decreases activity dramatically.These data suggest an important role for C16 esters and possibly the presence of a separate binding site on Na+, K+ -ATPase corresponding to the cardenolide C16 position.

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