4-Isopropylaniline
4-Isopropylaniline structure
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Common Name | 4-Isopropylaniline | ||
|---|---|---|---|---|
| CAS Number | 99-88-7 | Molecular Weight | 135.206 | |
| Density | 1.0±0.1 g/cm3 | Boiling Point | 225.6±9.0 °C at 760 mmHg | |
| Molecular Formula | C9H13N | Melting Point | -63 °C | |
| MSDS | Chinese USA | Flash Point | 92.2±0.0 °C | |
| Symbol |
GHS07 |
Signal Word | Warning | |
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Organo-palladium(II) complexes bearing unsymmetrical N,N,N-pincer ligands: synthesis, structures and oxidatively induced coupling reactions.
Dalton Trans. 44(16) , 7230-41, (2015) The 2-(2′-aniline)-6-imine-pyridines, 2-(C6H4-2′-NH2)-6-(CMe=NAr)C5H3N (Ar = 4-i-PrC6H4 (HL1a), 2,6-i-Pr2C6H3 (HL1b)), have been synthesised via sequential Stille cross-coupling, deprotection and condensation steps from 6-tributylstannyl-2-(2-methyl-1,3-dioxo... |
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O,N,N-pincer ligand effects on oxidatively induced carbon-chlorine coupling reactions at palladium.
Dalton Trans. 44(13) , 6040-51, (2015) The syntheses of two families of sterically tuneable O,N,N pro-ligands are reported, namely the 2-(phenyl-2'-ol)-6-imine-pyridines, 2-(C6H4-2'-OH),6-(CMe=NAr)C5H3N [Ar = 4-i-PrC6H4 (HL1(a)), 2,6-i-Pr2C6H3 (HL1(b))] and the 2-(phenyl-2'-ol)-6-(amino-prop-2-yl)... |
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Rapid mineralisation of the herbicide isoproturon in soil from a previously treated Danish agricultural field.
Pest Manag. Sci. 59(10) , 1118-24, (2003) Mineralisation of the phenylurea herbicide isoproturon (3-(4-isopropylphenyl)-1,1-dimethylurea) and two of its known metabolites, 3-(4-isopropylphenyl)-1-methylurea (monodesmethyl-isoproturon) and 4-isopropylaniline, was studied in Danish agricultural soils w... |
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Lewis acid double metal cyanide catalysts for hydroamination of phenylacetylene.
Chem. Commun. (Camb.) 47(14) , 4114-6, (2011) Double metal cyanides (DMCs) are highly active recyclable heterogeneous catalysts for hydroamination of phenylacetylene with 4-isopropylaniline. The best hydroamination yields are obtained with Zn-Co DMCs, especially if the particle size is decreased by a rev... |