28539-02-8 Usage
Uses
Catalyst for:Hydrolysis of phenyl esters of a-furoic acidUsed as:Corrosion inhibitor of iron in aerated acidic mediaReactive oxygen scavengerReactant for:Synthesis of hydroxy-skipped bis-homo-inositols as potential glycosidase inhibitors via Sharpless asymmetric dihydroxylation and substrate-directed anionic hydroxymethylationEnantioselective synthesis of aplysin utilizing a palladium-catalyzed addition of an arylboronic acid to an allenic alcohol, followed by Eschenmoser/Claisen rearrangementSynthesis of substituted dihydroquinoline carboxylic acids as antitumor and HIV-1 integrase inhibitorsGosteli-Claisen rearrangement
Check Digit Verification of cas no
The CAS Registry Mumber 28539-02-8 includes 8 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 5 digits, 2,8,5,3 and 9 respectively; the second part has 2 digits, 0 and 2 respectively.
Calculate Digit Verification of CAS Registry Number 28539-02:
(7*2)+(6*8)+(5*5)+(4*3)+(3*9)+(2*0)+(1*2)=128
128 % 10 = 8
So 28539-02-8 is a valid CAS Registry Number.
InChI:InChI=1/C7H7N3O/c11-5-10-7-4-2-1-3-6(7)8-9-10/h1-4,11H,5H2
28539-02-8Relevant articles and documents
N-Hydroxymethylation of 3-Aryl-2-cyanoprop-2-enethioamides
Chigorina, E. A.,Dotsenko, V. V.,Krivokolysko, S. G.
, p. 1411 - 1417 (2020/09/21)
Abstract: Hydroxymethylation of (E)-3-aryl-2-cyanoprop-2-enethioamides with an aqueous alcoholic solution of formaldehyde has afforded (E)-3-aryl-N-(hydroxymethyl)-2-cyanoprop-2-enethioamides. The predictive analysis of the biological activity of the obtained compounds in silico has been carried out.
