Chemistry:1,2-Dichloro-4-nitrobenzene
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Names | |
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Preferred IUPAC name
1,2-Dichloro-4-nitrobenzene | |
Other names
DCNB, 3,4-dichloronitrobenzene
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Identifiers | |
3D model (JSmol)
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PubChem CID
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UNII | |
UN number | 2811 1578 |
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Properties | |
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) |
organic solvents | |
Hazards | |
GHS pictograms | ![]() ![]() ![]() |
GHS Signal word | Danger |
H302, H336, H361, H372, H373, H411 | |
P201, P202, P260, P261, P264, P270, P271, P273, P281, P301+312, P304+340, P308+313, P312, P314, P330, P391, P403+233, P405, P501 | |
Flash point | 124 °C (255 °F; 397 K) |
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). | |
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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
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
![]() | Original source: https://en.wikipedia.org/wiki/1,2-Dichloro-4-nitrobenzene.
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