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2,5-Dichloroaniline

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This is an old revision of this page, as edited by Emeldir (talk | contribs) at 19:56, 15 September 2016 (preferred IUPAC name (PIN) according to ''Nomenclature of Organic Chemistry – IUPAC Recommendations and Preferred Names 2013 (Blue Book)''). The present address (URL) is a permanent link to this revision, which may differ significantly from the current revision.

2,5-Dichloroaniline
File:C6H3Cl2NH2.png
Names
Preferred IUPAC name
2,5-Dichloroaniline
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.002.233 Edit this at Wikidata
  • InChI=1S/C6H5Cl2N/c7-4-1-2-5(8)6(9)3-4/h1-3H,9H2
    Key: AVYGCQXNNJPXSS-UHFFFAOYSA-N
  • InChI=1/C6H5Cl2N/c7-4-1-2-5(8)6(9)3-4/h1-3H,9H2
    Key: AVYGCQXNNJPXSS-UHFFFAOYAK
  • C1=CC(=C(C=C1Cl)N)Cl
Properties
C6H5Cl2N
Molar mass 162.01 g·mol−1
Melting point 47 to 50 °C (117 to 122 °F; 320 to 323 K)
Boiling point 251 °C (484 °F; 524 K)
Except where otherwise noted, data are given for materials in their standard state (at 25 °C [77 °F], 100 kPa).

2,5-Dichloroaniline is an organic compound with the formula C6H3Cl2NH2. One of six isomers of dichloroaniline, it is a colorless solid that is insoluble in water. It is produced by hydrogenation of 1,4-dichloronitrobenzene.[1] It is a precursor to dyes and pigments, e.g., Pigment Yellow 10.[2]

Pigment Yellow 10, a derivative of 1,4-dichloroanilne, is commonly used for yellow road markings in the US.

References

  1. ^ Gerald Booth (2007). "Nitro Compounds, Aromatic" in Ullmann's Encyclopedia of Industrial Chemistry Wiley-VCH, Weinheim, 2005.
  2. ^ K. Hunger. W. Herbst "Pigments, Organic" in Ullmann's Encyclopedia of Industrial Chemistry, Wiley-VCH, Weinheim, 2012. doi:10.1002/14356007.a20_371
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