Via
condensations like the Henry reaction, nitroethene converts to several
compounds of bartering interest. Abstract with 3,4-dimethoxybenzaldehyde
affords the forerunner to the antihypertensive biologic methyldopa; abstract
with unsubstituted benzaldehyde yields phenyl-2-nitropropene. Nitroethane
condenses with two equivalents of formaldehyde to give, afterwards
hydrogenation, 2-amino-2-methyl-1,3-propanediol, which in about-face condenses
with oleic acid to accord an oxazoline, which protonates to accord a cationic
surfactant.
Like
some added nitrated amoebic compounds, nitroethane is aswell used as a
ammunition accretion and a forerunner to explosives.
Nitroethane
is a advantageous bread-and-butter for polymers such as polystyrene and is
decidedly advantageous for abandoning cyanoacrylate adhesives. In alcove
applications, it has been used as a basic in bogus attach remover and in aerial
beam adhesive sprays.
Nitroethane
has been used as a actinic feedstock in artful laboratories for amalgam of
controlled substances such as amphetamines.

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