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Decamethylene bromide

Thioethylene glycol, HSCH2CH2OH (prepared from ethylene oxide and hydrogen sulfide) is first reacted with sodium to give HOCHjCH SNa. It is then reacted with decamethylene bromide, BrlCHjliflBr to give tiadenol. [Pg.1476]

Decamethylene bromide was first prepared by heating the glycol in a sealed tube with fuming hydrobromic acid.1 3 Later it was prepared in the manner here described.2 3... [Pg.14]

Decamethylene bromide, 24 Decamethylene glycol, 25 Decane, i,io-dibromo-, 24 b-Decyl -bromobenzenesulfonate... [Pg.56]

Decamethylene bromide, 20, 24 Decamethylene glycol, 20, 25 Decane, 1,10-dibromo-, 20, 24 Decarboxylation, 23,18... [Pg.54]

The polymer may thus be counted as an addition polymer. A polymer which may be considered to be the same (if any differences in molecular weight are disregarded) can be formed from decamethylene bromide and sodium in the Wurtz reaction ... [Pg.22]

See other pages where Decamethylene bromide is mentioned: [Pg.1476]    [Pg.1626]    [Pg.57]    [Pg.13]    [Pg.72]    [Pg.24]    [Pg.25]    [Pg.115]    [Pg.3218]    [Pg.3218]    [Pg.992]    [Pg.1476]    [Pg.1476]    [Pg.1626]    [Pg.1476]    [Pg.1476]    [Pg.1626]    [Pg.1562]    [Pg.1889]    [Pg.28]   
See also in sourсe #XX -- [ Pg.20 , Pg.24 ]

See also in sourсe #XX -- [ Pg.20 , Pg.24 ]

See also in sourсe #XX -- [ Pg.20 , Pg.24 ]

See also in sourсe #XX -- [ Pg.20 , Pg.24 ]

See also in sourсe #XX -- [ Pg.24 ]

See also in sourсe #XX -- [ Pg.20 , Pg.24 ]

See also in sourсe #XX -- [ Pg.20 , Pg.24 ]

See also in sourсe #XX -- [ Pg.20 , Pg.24 ]

See also in sourсe #XX -- [ Pg.20 , Pg.24 ]

See also in sourсe #XX -- [ Pg.24 ]

See also in sourсe #XX -- [ Pg.20 , Pg.24 ]

See also in sourсe #XX -- [ Pg.20 , Pg.24 ]



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