nitroalkane


Also found in: Dictionary.
Related to nitroalkane: Nitro functional group

nitroalkane

[¦nī·trō′al‚kān]
(organic chemistry)
McGraw-Hill Dictionary of Scientific & Technical Terms, 6E, Copyright © 2003 by The McGraw-Hill Companies, Inc.
References in periodicals archive ?
The nitroalkane, nitroethane (10 mmol), was mixed with the Michael acceptor, methyl acrylate (10 mmol).
According to Golden Gate, Angus is the world's only chemical company dedicated to the manufacture and distribution of nitroalkanes and their derivatives.
Giri, "Fe-HCl: an efficient reagent for deprotection of oximes as well as selective oxidative hydrolysis of nitroalkenes and nitroalkanes to ketones," Synthetic Communications, vol.
The above-mentioned metals are deposited on the carbon support in a highly dispersed state, which decreases the hydrogen overvoltage and catalyses the reduction of nitroalkanes. These reactions take place on the metal-modified carbon electrodes at much more positive potentials than on carbon and at slightly more positive potentials than on the respective plain metallic electrodes [17].
His dissertation focused on the development of new catalytic methods for the preparation of chiral amines and nitroalkanes using diphosphine monoxide ligands.
Compounds that can be classified as combustion supporters but not as catalysts, for instance nitroalkanes, have been patented [103, 104].
Cueto and Pryor (5) recorded a similar phenomenon and reported that the yellow compound had Fourier-transform infrared spectroscopy (FT-IR)-based assignments from alkyl nitrates, nitroalkanes, and primary nitrocompounds.
For example, many marine sponges produce anti-fouling substances, such as nitroalkanes (which are made up of nitrogen, carbon, and hydrogen) isolated from the Okinawan sponge of the genus Theonella.
ANGUS is the world's only chemical company dedicated to the manufacture and distribution of nitroalkanes and their derivatives, which are versatile additives and intermediates that help customers to enhance their products' performance.
In aprotic solvents, at atmospheric pressure and room temperature, cobalt chelated with Schiff bases, catalyzes the oxygenation of indols, phenols, flavones, nitroalkanes, hydrazones, olefins, etc [8].
(4) Aldehydes 1,5-Pentanediol (Glutaraldehyde) 111-30-8 Carbamates 3-lodopropynylbutylcarbamate (IPBC) 55406-53-6 1-(3-Chloroallyl)-3,5,7-triaza-1- 4080-31 -3 azoniaadamantane chloride (CTAC) Formaldehyde 1,3-Dimethylol-5,5-dimethylhydantoin 6440-58-0 Releasing (DMDMH) Compounds 4,4-dimethyloxazolidine (DMO) 51200-87-4 1,2-Benzisothiazolin-3-one (BIT) 2634-33-5 HeterocyclicN, Mixture of 26172-55-4 S Compounds 5-chloro-2-methyl-4-isothiazolin-3-one and 2-methyl-4-isothiazolin-3-one (CMIT/MIT) 2-Methyl-4-isothiazolin-3-one (MIT) 2682-20-4 2-n-Octyl-4-isothiazolin-3-one (OIT) 26530-20-1 Hydroxymethyl 2-Bromo-2-nitropropane-1,3-diol 52-51-7 Nitroalkanes (Bronopol, BNPD) Classification Microbial pH range Min.