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3-Hydroxy-2-triaza-1,2-dien-2-ium-1-ylandrostan-17-one is a complex organic compound with a molecular formula of C21H34N3O2. It is a derivative of androstane, a steroid with a triaza-1,2-dien-2-ium-1-yl group attached to the 3-hydroxy position. 3-hydroxy-2-triaza-1,2-dien-2-ium-1-ylandrostan-17-one is characterized by its unique structure, which includes a steroidal core with a nitrogen-containing heterocycle. It is not a common chemical and may be of interest in specialized fields such as medicinal chemistry or organic synthesis. Due to its complexity, it is likely to have specific applications or properties that are not widely known, and further research would be required to understand its full potential and uses.

4817-43-0

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4817-43-0 Usage

Check Digit Verification of cas no

The CAS Registry Mumber 4817-43-0 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 4,8,1 and 7 respectively; the second part has 2 digits, 4 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 4817-43:
(6*4)+(5*8)+(4*1)+(3*7)+(2*4)+(1*3)=100
100 % 10 = 0
So 4817-43-0 is a valid CAS Registry Number.

4817-43-0SDS

SAFETY DATA SHEETS

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

Version: 1.0

Creation Date: Aug 20, 2017

Revision Date: Aug 20, 2017

1.Identification

1.1 GHS Product identifier

Product name (2S,3S,5S,8R,9S,10S,13S,14S)-2-azido-3-hydroxy-10,13-dimethyl-1,2,3,4,5,6,7,8,9,11,12,14,15,16-tetradecahydrocyclopenta[a]phenanthren-17-one

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:4817-43-0 SDS

4817-43-0Downstream Products

4817-43-0Relevant academic research and scientific papers

Synthesis of ferrocene-labeled steroids via copper-catalyzed azide-alkyne cycloaddition. Reactivity difference between 2β-, 6β- and 16β-azido-androstanes

Fehér, Klaudia,Balogh, János,Csók, Zsolt,Kégl, Tamás,Kollár, László,Skoda-F?ldes, Rita

experimental part, p. 738 - 744 (2012/07/03)

Copper-catalyzed cycloaddition of steroidal azides and ferrocenyl-alkynes were found to be an efficient methodology for the synthesis of ferrocene-labeled steroids. At the same time, a great difference between the reactivity of 2β- or 16β-azido-androstane

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