View source for 4-Bromoaniline

{{Orphan|date=June 2009}}
{{Chembox
| verifiedrevid = 298954318
| Reference = <ref>[http://www.chemblink.com/products/106-40-1.htm 4-Bromoaniline], Chemblink.com</ref>
| ImageFileL1 = 4-Bromoaniline.svg
| ImageSizeL1 = 80px
| ImageFileR1 = 4-bromoaniline-from-xtal-2003-3D-balls.png
| ImageSizeR1 = 120px
| IUPACName = 4-bromoaniline
| OtherNames = ''p''-bromoaniline, 4-bromobenzenamine, ''p''-bromophenylamine
| Section1 = {{Chembox Identifiers
| CASNo_Ref = {{cascite}}
| CASNo = 106-40-1
| EINECS = 203-393-9
| PubChem = 
| SMILES = }}
| Section2 = {{Chembox Properties
| Formula = C<sub>6</sub>H<sub>6</sub>BrN
| MolarMass = 172.02&nbsp;g&nbsp;mol<sup>−1</sup>
| Appearance = 
| Density = 1.5 g/cm<sup>3</sup>
| MeltingPt = 60-64 ºC
| BoilingPt = 
| Solubility = <0.1 g/100 mL at 23 ºC }}
| Section3 = {{Chembox Hazards
|   ExternalMSDS = [http://msds.chem.ox.ac.uk/BR/p-bromoaniline.html External MSDS]
|   RPhrases = {{R20/21/22}} {{R36/37/38}}
|   SPhrases = {{S26}} {{S36/37/39}}
| MainHazards = 
| FlashPt = 
| Autoignition = }}
}}

'''4-Bromoaniline''' is a compound where an [[aniline]] molecule is substituted with a [[bromine]] atom. Commercially available, this compound may be used as a building block, e.g. in the preparation of p-bromo[[biphenyl]] via the [[Gomberg-Bachmann reaction]].<ref>{{OrgSynth | prep = cv1p0113 | collvol = 1 | collvolpages = 113 | author = [[Moses Gomberg|M. Gomberg]] and [[Werner Emmanuel Bachmann|W. E. Bachmann]] | year = 1941 | title = p-Bromobiphenyl}}</ref>

== References ==
{{reflist}}

{{DEFAULTSORT:Bromoaniline, 4-}}
[[Category:Aromatic amines]]

[[de:Bromaniline]]
[[it:4-bromoanilina]]
[[Category:2Fix]]