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4-chloroaniline

4-Chloroaniline
4-Chloranilin.svg
Names
Preferred IUPAC name
4-Chloroaniline
Systematic IUPAC name
4-Chlorobenzenamine
Other names
p-Chloroaniline
Identifiers
106-47-8 YesY
3D model (Jmol) Interactive image
ChEBI CHEBI:20331 N
ChEMBL ChEMBL15888 N
ChemSpider 7524 YesY
ECHA InfoCard 100.003.093
KEGG C14450 YesY
PubChem 7812
UNII Z553SGH315 N
Properties
C6H6ClN
Molar mass 127.57154 g/mol
Appearance pale yellow solid
Density 1.43 g·cm−3
Melting point 72.5 °C (162.5 °F; 345.6 K)
Boiling point 232 °C (450 °F; 505 K)
2.6 g/litre at 20 °C (Scheunert, 1981)
Hazards
Main hazards Very toxic, possible carcinogen. Absorbed through skin.
Safety data sheet External MSDS
Flash point 113 °C (235 °F; 386 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).
N  (what is YesYN ?)
Infobox references

4-Chloroaniline is an organochlorine compound with the formula ClC6H4NH2. This pale yellow solid is one of several known chloroanilines.

4-Chloroaniline is not prepared from aniline, which tends to overchlorinate. Instead, it is prepared by hydrogenation of 4-nitrochlorobenzene, which in turn is prepared by nitration of chlorobenzene.

4-Chloroaniline is an important building block used in the chemical industry for the production of pesticides, drugs, and dyestuffs. It is a precursor to the widely used antimicrobial and bacteriocide chlorhexidine and is used in the manufacture of pesticides, including pyraclostrobin, anilofos, monolinuron and chlorphthalim. Some benzodiazepine drugs use 4-chloroaniline in their manufacture.

4-Chloroaniline can be used to make dorastine (antihistamine), lorcainide (antiarrhythmic) and Ontianil.


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Wikipedia

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