Simultaneous azo-coupling method for steroid acetate hydrolyzing enzyme

1983 ◽  
Vol 77 (1) ◽  
pp. 99-104 ◽  
Author(s):  
S. Partanen
Keyword(s):  
1961 ◽  
Vol 1961 (2) ◽  
pp. 111-115 ◽  
Author(s):  
Kensaku KAWAKATSU ◽  
Masahiko MORI ◽  
Yasuo DEGUCHI ◽  
Tsuneo MIZUSHIMA
Keyword(s):  

1982 ◽  
Vol 47 (10) ◽  
pp. 2746-2748 ◽  
Author(s):  
Miroslav Matrka ◽  
Jana Pípalová

Oxidation of Trypan Blue with cerium(IV) ion in acid medium gives arenediazonium cation similar to the oxidation product of N,N-dimethyl-4-aminoazobenzene. Quantitative evaluation of the arenediazonium salt formed has been carried out spectrophotometrically after previous C-azo coupling with 2-naphthol.


Molbank ◽  
10.3390/m1238 ◽  
2021 ◽  
Vol 2021 (2) ◽  
pp. M1238
Author(s):  
Ion Burcă ◽  
Valentin Badea ◽  
Calin Deleanu ◽  
Vasile-Nicolae Bercean

A new azo compound was prepared via the azo coupling reaction between 4-(ethoxycarbonyl)-3-methyl-1H-pyrazole-5-diazonium chloride and 8-hydroxyquinoline (oxine). The ester functional group of the obtained compound was hydrolyzed and thus a new chemical structure with a carboxylic functional group resulted. The structures of the new compounds were fully characterized by: UV–Vis, FT-IR, 1D and 2D NMR spectroscopy, and HRMS spectrometry.


Sign in / Sign up

Export Citation Format

Share Document