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DIGOXIGENIN-3,12-DIACETATE is a chemical with a specific purpose. Lookchem provides you with multiple data and supplier information of this chemical.

6078-59-7

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6078-59-7 Usage

Definition

ChEBI: A steroid ester that is the 3,12-diacetyl derivative of digoxigenin.

Check Digit Verification of cas no

The CAS Registry Mumber 6078-59-7 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 6,0,7 and 8 respectively; the second part has 2 digits, 5 and 9 respectively.
Calculate Digit Verification of CAS Registry Number 6078-59:
(6*6)+(5*0)+(4*7)+(3*8)+(2*5)+(1*9)=107
107 % 10 = 7
So 6078-59-7 is a valid CAS Registry Number.
InChI:InChI=1/C27H38O7/c1-15(28)33-19-7-9-25(3)18(12-19)5-6-21-22(25)13-23(34-16(2)29)26(4)20(8-10-27(21,26)31)17-11-24(30)32-14-17/h11,18-23,31H,5-10,12-14H2,1-4H3/t18-,19+,20-,21?,22?,23-,25+,26+,27+/m1/s1

6078-59-7SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 17, 2017

Revision Date: Aug 17, 2017

1.Identification

1.1 GHS Product identifier

Product name digoxigenin 3,12-diacetate

1.2 Other means of identification

Product number -
Other names digitoxigenin

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

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:6078-59-7 SDS

6078-59-7Relevant academic research and scientific papers

17BETA-HETEROCYCLYL-DIGITALIS LIKE COMPOUNDS FOR THE TREATMENT OF HEART FAILURE

-

Page/Page column 0149; 0152, (2020/02/13)

Disclosed are compounds of formula (I) wherein X, Y, Z are annular atoms comprised in a five-membered carbocyclic or heterocyclic ring, selected from the group consisting of CH, NH, N, O, S; said carbocyclic or heterocyclic ring being optionally substituted with amino (C1-C4) linear or branched alkyl or guanidine or guanidino (C1-C4) linear or branched alkyl; with the proviso that the heterocycle ring is not furyl; n is 0 or 1; R is H or OH; the dotted line represents an optional double bond C=C; the thick line represents a bond in the β configuration; the wavy line represents a bond both in the α and β configuration; their enantiomeric and/or diastereomeric mixtures, their pharmaceutically acceptable salts, their solvates, hydrates; their metabolite and metabolic precursors. The compounds of formula (I) are for use as medicaments, in particular for the treatment of acute or chronic heart failure. Oral administration is also possible.

Partial Syntheses of Cardenolides and Cardenolide Analogues. XIII. Synthesis of Substituted 14,21-Epoxy-5&β,14&β-card-20(22)-enolides

Courault, Klaus,Lindig, Claus

, p. 445 - 452 (2007/10/02)

The 12-substituted 14,21-epoxy-5β,14β-card-20(22)-enolides 3 and 5 were synthesized by oxidation of the appropriate 17β-(3-furyl) derivatives 2b and 2c, respectively, with chromic acid. 5 was converted to the conjugated Δ9(11)-12-ketone 6 by dehydrogenation with selenium dioxide.The biological activities of the new compounds were investigated and are discussed.

13C NMR Spectra of 5β,14β-Hydroxysteroids

Habermehl, Gerhard G.,Hammann, Peter E.,Wray, Victor

, p. 959 - 963 (2007/10/02)

The 13C chemical shifts of 30 substituted 5β,14β-hydroxysteroids are described and discussed.Substituent chemical shifts for 12α- and 12β-hydroxy groups were evaluated, and interesting γ effects were observed.A correlation is shown to exist between the 1H shifts of H-17 and the 13C shifts of C-17 for various C-12 substituents.A relationship for the distance of the substituent at C-12 from H-17 in the 14β,20-lactones was demonstrated, where an increased distance between these atoms is associated with smaller shift differences.

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