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5- Methyl-4-nitrobenzofuroxan

Nitro groups in the 4-position may also participate in the rearrangement. For example, 5-chloro- and 5-methyl-4-nitrobenzofuroxans rearrange to their 7-chloro- and 7-methyl-4-nitro isomers, the ease of the process being attributed to steric inhibition of resonance for the nitro group in the starting materials. Similarly, 4-ethoxycarbonylamino-5,7-dinitroben-zofuroxan equilibrates with its 4,6-dinitro-5-urethane isomer. [Pg.408]


See other pages where 5- Methyl-4-nitrobenzofuroxan is mentioned: [Pg.37]    [Pg.318]    [Pg.152]    [Pg.40]    [Pg.291]    [Pg.9]    [Pg.10]    [Pg.11]    [Pg.37]    [Pg.318]    [Pg.240]    [Pg.244]    [Pg.258]    [Pg.411]    [Pg.152]    [Pg.411]    [Pg.183]    [Pg.295]    [Pg.40]    [Pg.291]    [Pg.571]   


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5- Methyl-4-nitrobenzofuroxan rearrangement

Nitrobenzofuroxans

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