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Names | |
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Preferred IUPAC name
2,6-Dichloroaniline | |
Identifiers | |
3D model (
JSmol)
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ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.009.237 |
EC Number |
|
PubChem
CID
|
|
UNII | |
UN number | 1590 |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C6H5Cl2N | |
Molar mass | 162.01 g·mol−1 |
Appearance | white solid |
Melting point | 39 °C (102 °F; 312 K) |
Hazards | |
GHS labelling: | |
![]() ![]() ![]() ![]() | |
Danger | |
H301, H311, H317, H331, H373, H410 | |
P260, P261, P264, P270, P271, P272, P273, P280, P301+P310, P302+P352, P304+P340, P311, P312, P314, P321, P322, P330, P333+P313, P361, P363, P391, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
2,6-Dichloroaniline is an organic compound with the formula C6H3Cl2(NH2). It is one of several isomers of dichloroaniline. It is a colorless or white solid. Derivatives include the drugs clonidine and diclofenac.
It is produced by hydrogenation of 2,6-dichloronitrobenzene. [1]
In the laboratory, it can be prepared by halogenation of sulfanilamide followed by desulfonation. [2]
![]() | |
Names | |
---|---|
Preferred IUPAC name
2,6-Dichloroaniline | |
Identifiers | |
3D model (
JSmol)
|
|
ChEMBL | |
ChemSpider | |
ECHA InfoCard | 100.009.237 |
EC Number |
|
PubChem
CID
|
|
UNII | |
UN number | 1590 |
CompTox Dashboard (
EPA)
|
|
| |
| |
Properties | |
C6H5Cl2N | |
Molar mass | 162.01 g·mol−1 |
Appearance | white solid |
Melting point | 39 °C (102 °F; 312 K) |
Hazards | |
GHS labelling: | |
![]() ![]() ![]() ![]() | |
Danger | |
H301, H311, H317, H331, H373, H410 | |
P260, P261, P264, P270, P271, P272, P273, P280, P301+P310, P302+P352, P304+P340, P311, P312, P314, P321, P322, P330, P333+P313, P361, P363, P391, P403+P233, P405, P501 | |
Except where otherwise noted, data are given for materials in their
standard state (at 25 °C [77 °F], 100 kPa).
|
2,6-Dichloroaniline is an organic compound with the formula C6H3Cl2(NH2). It is one of several isomers of dichloroaniline. It is a colorless or white solid. Derivatives include the drugs clonidine and diclofenac.
It is produced by hydrogenation of 2,6-dichloronitrobenzene. [1]
In the laboratory, it can be prepared by halogenation of sulfanilamide followed by desulfonation. [2]