NITRATION OF PARAFFINS. DETERMINATION OF NITRO GROUP POSITION IN SECONDARY NITROHEPTANE**Paper LXV in the series “Aliphatic Nitro Compounds”.

1964 ◽  
pp. 19-25
Author(s):  
W. BIERNACKI ◽  
T. URBAŃSKI
Keyword(s):  
Nitro Group ◽  
Nitro Compounds ◽  
Aliphatic Nitro Compounds ◽  
Group Position

The possibilities of polarography in the chemistry of nitroazoles

1984 ◽  
Vol 49 (6) ◽  
pp. 1342-1353 ◽  
Author(s):  
Dragica Dumanović ◽  
Janka Ćirić ◽  
Djuro Kosanović ◽  
Dragoslav Jeremić
Keyword(s):  
Nitro Group ◽  
Systematic Investigation ◽  
Nitro Compounds ◽  
The Other ◽  
Polarographic Method ◽  
Spectrophotometric Methods ◽  
Group Position ◽  
High Yields

Based on systematic investigation of mononitroimidazoles, selective polarographic and spectrophotometric methods for determination of nitrazole compounds in reaction mixture are proposed. It was proved that the selectivity is based on the different properties of the nitro group due to the effects of the nitro group position in the ring, the type and position of the other substituents and on the fact whether the compound is N-substituted or not. The proposed methods can be successfully used for monitoring the synthetic procedures and decreasing the number of experiments for optimization. Based on the anticipated and proved behaviour of the nitro compounds of pyrazole, novel mononitropyrazole derivatives were synthetized in a new way and with high yields. Applying the polarographic method it was discovered that during N-substitution of tautomeric mononitroimidazole and mononitropyrazole substrates other byproducts were obtained besides the main products and undesired isomers. The products were identified and then a correct and more complete N-substitution scheme could be given. Following quantitatively these N-substitution processes conclusions which directly concern the mechanism of reactions were drawn.

1H, 13C and 15N NMR Spectra of Coupling Products of Benzenediazonium Salts with Aliphatic Nitro Compounds and Study of Their E/Z Isomerism

1996 ◽  
Vol 61 (4) ◽  
pp. 589-596 ◽  
Author(s):  
Antonín Lyčka
Keyword(s):  
Dimethyl Sulfoxide ◽  
Nmr Spectra ◽  
Chemical Shifts ◽  
Nitro Compounds ◽  
Coupling Constants ◽  
15N Nmr ◽  
Geometrical Isomers ◽  
Sodium Salts ◽  
Aliphatic Nitro Compounds ◽  
Tautomeric Forms

The 1H, 13C and 15N NMR spectra have been measured of coupling products of benzenediazonium salts with nitromethane, nitroethane, 1-nitropropane, 2-nitroethanol and of their sodium salts, and the chemical shifts have been unambiguously assigned. The coupling products have been found to exist only in their hydrazone tautomeric forms. Stereospecific behaviour of the coupling constants 2J(15N,1H) and 2J(15N,13C) in the 15N isotopomers and NOESY have been used to differentiate between the E and Z geometrical isomers. The above-mentioned compounds exist as Z isomers in deuteriochloroform and predominantly (>95%) as E isomers in dimethyl sulfoxide, while the sodium salts are present only as E isomers in dimethyl sulfoxide.

Colorimetric Determination of Aklomide (2-Chloro-4-Nitrobenzamide) in Poultry Feed

1969 ◽  
Vol 52 (3) ◽  
pp. 438-441
Author(s):  
Glenn M George ◽  
A C Daftsios ◽  
Joseph L Morrison
Keyword(s):  
Nitro Group ◽  
Poultry Feed ◽  
Colorimetric Determination ◽  
Average Recovery ◽  
Low Level ◽  
Color Development ◽  
Titanium Trichloride ◽  
High Level

Abstract The coccidiostat aklomide is extracted from feed with methanol and assayed colorimetrically by reduction of the nitro group to anamine with titanium trichloride and subsequent color development with t he Bratton-Marshall reaction. Thirteen laboratories studied the method collaboratively on two levels of medicated feed. Overall average recovery was 106.5% of the oretical for the low level and 104.5% of the oretical for the high level. The method is recommended for adoption as official first action

Synthesis and antimicrobial activity of aliphatic nitro compounds

1974 ◽  
Vol 17 (9) ◽  
pp. 977-981 ◽  
Author(s):  
Nigel G. Clark ◽  
Betty Croshaw ◽  
Brian E. Leggetter ◽  
David F. Spooner
Keyword(s):  
Antimicrobial Activity ◽  
Nitro Compounds ◽  
Aliphatic Nitro Compounds
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