Dodecane, 1-bromo

Sigma TCI Am. http //www.tciamerica.com Dodecane, 1-bromo. See,Lauryl bromide 1,2-Dodecane carbonate... 

CAS 143-15-7 EINECS/ELINCS 205-587-9 Synonyms 1-Bromododecane Dodecane, 1-bromo Dodecyl bromide n-Dodecyl bromide... 

Dodecanaminium, N,N-dimethyl-N-(3-(wheat-protein-hydrolysate) propyl)-, chloride. See Laurdimonium hydroxypropyl hydrolyzed wheat protein 1-Dodecanaminium, N-[2-(dodecyloxy)-2-oxyethyl]-N,N-dimethyl, chloride. See Dilauryl acetyl dimonium chloride Dodecane, 1-bromo. See Lauryl bromide... 

Trialkylsilanes are generally more effective than dialkyl- or monoalkylsilanes in minimizing isomerizations. The reduction of 2-bromododecane to dodecane proceeds under aluminum chloride catalysis in 82% yield using n-butylsilane and in 87% yield with tri-n-butylsilane.186 However, similar treatment of bromo-cycloheptane with triethylsilane yields a mixture of 39% cycloheptane and 26% methylcyclohexane. The same substrate yields 65% methylcyclohexane and less than 1% cycloheptane when n -butylsilane is the reducing agent.186... 

P 15] The reservoir of the dielectrophoretic droplet mixer was filled with 1-bromo-dodecane, a low-permittivity, low-viscosity, water-immiscible hydrocarbon [99]. AC signals of up to 180 Vp p and frequencies between 5 and 500 kHz were formed using a programmable function generator and amplified by variable gain amplifiers. 

Photoreactions of Thymines etc. - The uracil derivative (184) undergoes photochemical transformation when it is irradiated in frozen benzene with added trifluoroacetic acid. Cyclodimerization occurs yielding derivatives of diaza-pentacyclo[6.4.0.0 . 0 . 0 ]dodecane derivatives such as (185). Other addition products (186) and (187) were also identified. The photoreduction of 5-bromo-uracil (188) has been studied. ... 

Jin et al. [229] further performed the dehydrohalogenation of 2-bromo-octane with dodecane as the organic solvent and potassium hydroxide in the aqueous solution to investigate the synergistic effect of two PT catalysts in the situation of a third liquid phase using a combination of tetrahexylammonium bromide and PEG. They concluded that a molecule of tetrahexylammonium bromide surrounded by many molecules of water and some PEG 200 led to the effect of water on the catalytic activity of tetrahexylammonium bromide becoming weaker when the amount of PEG was increased. 

Aromatic amines have been alkylated using benzyl bromide and 1-bromo-dodecane in variable yields using a PEG methylether as the PTC [149]. 

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