1,2-Dichloro-4-nitrobenzene

1,2-Dichloro-4-nitrobenzene
Names
	Preferred IUPAC name 1,2-Dichloro-4-nitrobenzene
	Other names DCNB, 3,4-dichloronitrobenzene
Identifiers
CAS Number	99-54-7 [chemspider];
3D model (JSmol)	Interactive image;
ChEMBL	ChEMBL167468 ;
ChemSpider	21106095 ;
ECHA InfoCard	100.002.513
EC Number	202-764-2;
PubChem CID	7443;
RTECS number	CZ5250000;
UNII	IJT74JI7FS;
UN number	2811 1578
CompTox Dashboard (EPA)	DTXSID8024999 ;
	InChI InChI=1S/C6H3Cl2NO2/c7-5-2-1-4(9(10)11)3-6(5)8/h1-3H Key: NTBYINQTYWZXLH-UHFFFAOYSA-N ; InChI=1/C6H3Cl2NO2/c7-5-2-1-4(9(10)11)3-6(5)8/h1-3H Key: NTBYINQTYWZXLH-UHFFFAOYAQ;
	SMILES Clc1ccc(cc1Cl)[N+]([O-])=O;
Properties
Chemical formula	C6H3Cl2NO2
Molar mass	192.01
Appearance	colourless to yellow needles
Density	1.4588 g/cm3
Melting point	52.8 to 56 °C (127.0 to 132.8 °F; 325.9 to 329.1 K)
Boiling point	263 °C (505 °F; 536 K)
Solubility in water	organic solvents
Hazards
	GHS labelling:
Pictograms
Signal word	Danger
Hazard statements	H302, H336, H361, H372, H373, H411
Precautionary statements	P201, P202, P260, P261, P264, P270, P271, P273, P281, P301+P312, P304+P340, P308+P313, P312, P314, P330, P391, P403+P233, P405, P501
Flash point	124 °C (255 °F; 397 K)
Autoignition; temperature	420 °C (788 °F; 693 K)
	Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa). verify (what is ?) Infobox references

1,2-Dichloro-4-nitrobenzene is an organic compound with the formula 1,2-Cl₂C₆H₃-4-NO₂. This pale yellow solid is related to 1,2-dichlorobenzene by the replacement of one H atom with a nitro functional group. This compound is an intermediate in the synthesis of agrochemicals.

Production and uses[edit]

The nitration of 1,2-dichlorobenzene mainly produces 1,2-dichloro-4-nitrobenzene, together with smaller amounts of the 3-nitro isomer. It can also be prepared by chlorination of 1-chloro-4-nitrobenzene.^[1]

One of the chlorides is reactive toward nucleophiles. Potassium fluoride gives 2-chloro-1-fluoro-4-nitrobenzene, an intermediate in the production of herbicides. With ammonia, one obtains 2-chloro-4-nitroaniline, a precursor to diazo dyes. Reduction with iron powder gives 3,4-dichloroaniline (m.p. 72 °C, CAS# 95-76-1).^[1]

References[edit]

^ ^a ^b Gerald Booth (2007). "Nitro Compounds, Aromatic" in Ullmann's Encyclopedia of Industrial Chemistry Wiley-VCH, Weinheim, 2005.

[Booth-1] Gerald Booth (2007). "Nitro Compounds, Aromatic" in Ullmann's Encyclopedia of Industrial Chemistry Wiley-VCH, Weinheim, 2005.

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