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2-Butanone 1.3- dibromo-3-methyl

BUTANONE, 1 bromo 3 methyl, 55, 24 2 Butanone, 3-bromo-3-methyl-, 55, 25 2-Butanone, 1,3-dibromo-3-methyl-, 58, 22,... [Pg.179]

The dithiolanone was prepared by Luhmann et al. (1977) by treatment of l,3-dibromo-3-methyl-2-butanone with sodium sulfide (together with another cyclization product, the thietanone). [Pg.342]

See other pages where 2-Butanone 1.3- dibromo-3-methyl is mentioned: [Pg.114] [Pg.115] [Pg.61] [Pg.61] [Pg.78] [Pg.29] [Pg.114] [Pg.115] [Pg.24] [Pg.714] [Pg.61] [Pg.13] [Pg.101] [Pg.61] [Pg.61] [Pg.106]

See also in sourсe #XX -- [ Pg.920 ]

See also in sourсe #XX -- [ Pg.22 , Pg.24 , Pg.58 ]

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1.1- dibromo-2-methyl

2- Butanone, 1,3-dibromo

3- Methyl-2-butanone

Butanon

Butanone