![]() 3-Bromoaniline structure
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Common Name | 3-Bromoaniline | ||
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CAS Number | 591-19-5 | Molecular Weight | 172.023 | |
Density | 1.6±0.1 g/cm3 | Boiling Point | 251.0±0.0 °C at 760 mmHg | |
Molecular Formula | C6H6BrN | Melting Point | 16.8 °C | |
MSDS | Chinese USA | Flash Point | 101.2±19.8 °C | |
Symbol |
![]() GHS07 |
Signal Word | Warning |
Two-step hollow fiber-based, liquid-phase microextraction combined with high-performance liquid chromatography: a new approach to determination of aromatic amines in water.
J. Chromatogr. A. 1082(2) , 136-42, (2005) A novel method for the extraction of aromatic amines present in water samples is produced here coupling two-step liquid-phase microextraction with high performance liquid chromatography by using a monolithic column. The hydrophobic porous polypropylene membra... |
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m-[125I]iodoaniline: a useful reagent for radiolabeling biotin.
Int. J. Rad. Appl. Instrum. B 19(3) , 297-301, (1992) Biotinyl-m-[125I]iodoanilide (BIA) was synthesized by coupling biotin to m-[125I]iodoaniline via a mixed anhydride reaction. m-[125I]Iodoaniline was produced from the tin precursor, which was prepared using a palladium catalyzed reaction of hexabutylditin wit... |
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Cobb JM, et al.
Tetrahedron Lett. 40(5) , 1045-1048, (1999)
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Acute renal and hepatic effects induced by 3-haloanilines in the Fischer 344 rat.
J. Appl. Toxicol. 15(2) , 139-46, (1995) Haloanilines are commonly used as chemical intermediates in the manufacture of a wide range of products. The purpose of this study was to examine the in vivo nephrotoxic and hepatotoxic potentials of the 3-haloanilines. The in vitro effects of the 3-haloanili... |
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A general palladium-catalyzed carbonylative synthesis of 2-alkylbenzoxazinones from 2-bromoanilines and acid anhydrides.
Chemistry 18(40) , 12599-602, (2012) (C), its (O)K! An efficient palladium-catalyzed carbonylative synthesis of 2-alkylbenzoxazinones has been developed. By starting from 2-bromoanilines and acid anhydrides, the corresponding products were isolated in good yields.Copyright © 2012 WILEY-VCH Verla... |
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