![cover image](https://wikiwandv2-19431.kxcdn.com/_next/image?url=https://upload.wikimedia.org/wikipedia/commons/thumb/7/70/4-bromoaniline-from-xtal-2003-3D-balls.png/640px-4-bromoaniline-from-xtal-2003-3D-balls.png&w=640&q=50)
4-Bromoaniline
Chemical compound / From Wikipedia, the free encyclopedia
4-Bromoaniline is a compound where an aniline molecule is substituted with a bromine atom on the para position. Commercially available, this compound may be used as a building block, e.g. in the preparation of monobrominated biphenyl via the Gomberg-Bachmann reaction.[2]
Quick Facts Names, Identifiers ...
| |||
Names | |||
---|---|---|---|
Preferred IUPAC name
4-Bromoaniline | |||
Other names
| |||
Identifiers | |||
| |||
3D model (JSmol) |
|||
ChEMBL | |||
ChemSpider |
| ||
ECHA InfoCard | 100.003.086 ![]() | ||
EC Number |
| ||
PubChem CID |
|||
RTECS number |
| ||
UNII | |||
UN number | 2811 | ||
CompTox Dashboard (EPA) |
|||
| |||
| |||
Properties | |||
C6H6BrN | |||
Molar mass | 172.025 g·mol−1 | ||
Density | 1.5 g/cm3 | ||
Melting point | 60 to 64 °C (140 to 147 °F; 333 to 337 K) | ||
<0.1 g/100 mL at 23 °C | |||
-84.06·10−6 cm3/mol | |||
Hazards | |||
GHS labelling: | |||
![]() ![]() ![]() | |||
Danger | |||
H302, H311, H315, H319, H332, H335, H373 | |||
P260, P261, P264, P270, P271, P280, P301+P312, P302+P352, P304+P312, P304+P340, P305+P351+P338, P312, P314, P321, P322, P330, P332+P313, P337+P313, P361, P362, P363, P403+P233, P405, P501 | |||
Safety data sheet (SDS) | External MSDS | ||
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
|
Close