2,5-Dichloroaniline

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2,5-Dichloroaniline
2,5-Dichloranilin.svg
Names
Preferred IUPAC name
2,5-Dichloroaniline
Identifiers
3D model (JSmol)
ChemSpider
ECHA InfoCard 100.002.233 OOjs UI icon edit-ltr-progressive.svg
PubChem CID
UNII
  • 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-dichloro-2-nitrobenzene. [1] It is a precursor to dyes and pigments, e.g., Pigment Yellow 10. [2]

Pigment Yellow 10, a derivative of 2,5-dichloroanilne, is commonly used for yellow road markings in the US. Yellow road marking.jpg
Pigment Yellow 10, a derivative of 2,5-dichloroanilne, is commonly used for yellow road markings in the US.

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3,4-Dichloroaniline is an organic compound with the formula C6H3Cl2(NH2). It is one of several isomers of dichloroaniline. It is a white solid although commercial samples often appear gray. It is a precursor to dyes, agricultural chemicals, and drugs including the antimalarial chlorproguanil and the herbicides propanil, linuron, DCMU, and diuron.

<span class="mw-page-title-main">2,3-Dichloroaniline</span> Chemical compound

2,3-Dichloroaniline is an organic compound with the formula C6H3Cl2(NH2). It is one of several isomers of dichloroaniline. It is a colorless oil although commercial samples often appear colored. It is produced by hydrogenation of 2,3-dichloronitrobenzene.

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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