21497-13-2 Usage
Organic compound
NMPP is an organic compound, meaning it is primarily composed of carbon atoms and hydrogen atoms, and may also contain other elements such as oxygen and nitrogen.
Inhibits enzymes
NMPP is used as a pharmacological tool to inhibit enzymes, which are proteins that catalyze chemical reactions in the body.
Therapeutic potential
NMPP has been studied for its potential as a therapeutic agent for a variety of medical conditions, including cancer and inflammatory diseases.
Valuable research tool
The chemical structure and properties of NMPP make it a valuable tool for research into potential therapeutic interventions.
Possible development of new medications
Due to its unique properties, NMPP could hold promise for the development of new medications in the future.
Check Digit Verification of cas no
The CAS Registry Mumber 21497-13-2 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,1,4,9 and 7 respectively; the second part has 2 digits, 1 and 3 respectively.
Calculate Digit Verification of CAS Registry Number 21497-13:
(7*2)+(6*1)+(5*4)+(4*9)+(3*7)+(2*1)+(1*3)=102
102 % 10 = 2
So 21497-13-2 is a valid CAS Registry Number.
21497-13-2Relevant academic research and scientific papers
Z-Selective phosphine promoted 1,4-reduction of ynoates and propynoic amides in the presence of water
Drikermann, Denis,Kupfer, Stephan,Seifert, Fabian,Steinmetzer, Johannes,Vilotijevic, Ivan,Zi, You
, p. 6092 - 6097 (2021/07/21)
Phosphine-mediated reductions of substituted propynoic esters and amides in the presence of water yield the partially reduced α,β-unsaturated esters and amides with highZ-selectivity. The competitivein situ ZtoE-isomerization of the product in some cases lowers theZtoEratios of the isolated α,β-unsaturated carbonyl products. Reaction time and the amounts of phosphine and water in the reaction mixture are the key experimental factors which control the selectivity by preventing or reducing the rates ofZ- toE-product isomerization. Close reaction monitoring enables isolation of theZ-alkenes with high selectivities. The computational results suggest that the reactions could be highlyZ-selective owing to the stereoselective formation of theE-P-hydroxyphosphorane intermediate.
