4-Bromotoluene
4-Bromotoluene structure
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Common Name | 4-Bromotoluene | ||
|---|---|---|---|---|
| CAS Number | 106-38-7 | Molecular Weight | 171.035 | |
| Density | 1.4±0.1 g/cm3 | Boiling Point | 183.8±9.0 °C at 760 mmHg | |
| Molecular Formula | C7H7Br | Melting Point | 26-29 °C(lit.) | |
| MSDS | Chinese USA | Flash Point | 85.0±0.0 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Tetragonal Cu2Se nanoflakes: synthesis using selenated propylamine as Se source and activation of Suzuki and Sonogashira cross coupling reactions.
Dalton Trans. 44(2) , 725-32, (2014) The metastable tetragonal Cu2Se phase as nanoflakes has been synthesized for the first time by treating CuCl2 taken in a mixture (1:1) of 1-octadecene and oleylamine with H2N-(CH2)3-SePh dissolved in 1-octadecene. Powder X-ray diffraction (PXRD), HRTEM, SEM-E... |
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Possible intermediates of Cu(phen)-catalyzed C-O cross-coupling of phenol with an aryl bromide by in situ ESI-MS and EPR studies.
Dalton Trans. 43(29) , 11410-7, (2014) The C-O coupling reaction between 2,4-dimethylphenol and 4-bromotoluene catalyzed by the CuI/K2CO3/phen system can be inhibited by the radical scavenger cumene. Complexes [Cu(i)(phen)(1-(2,4-dimethylphenoxy)-4-methylbenzene)](+) (denoted as A), {H[Cu(i)(phen)... |
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Fluorogenic derivatization of aryl halides based on the formation of biphenyl by Suzuki coupling reaction with phenylboronic acid
J. Chromatogr. A. 1216(40) , 6873-6, (2009) The fluorogenic derivatization method for aryl halide was developed for the first time. This method was based on the formation of fluorescent biphenyl structure by Suzuki coupling reaction between aryl halides and non-fluorescent phenylboronic acid (PBA). We ... |
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Synthesis of ketones from alpha-oxocarboxylates and aryl bromides by Cu/Pd-catalyzed decarboxylative cross-coupling.
Angew. Chem. Int. Ed. Engl. 47(16) , 3043-5, (2008)
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Successful application of microstructured continuous reactor in the palladium catalysed aromatic amination. Mauger C, et al.
J. Organomet. Chem. 690(16) , 3627-29, (2005)
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Triaryl phosphine-functionalized N-heterocyclic carbene ligands for Heck reaction. Wang A-E, et al.
Tetrahedron 61(1) , 259-66, (2005)
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