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2,5-dichloro-4-nitrophenol

  • Name 2,5-dichloro-4-nitrophenol
  • CAS 5847-57-4
  • Purity 99%
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1.What is the 2,5-dichloro-4-nitrophenol ?

2,5-dichloro-4-nitrophenol is an organic compound characterized by the presence of two chlorine atoms at the 2nd and 5th carbon positions and a nitro group at the 4th carbon position on a phenol ring. This yellow crystalline solid is known for its potential use as a chemical intermediate in the synthesis of various pesticides and herbicides. It is also recognized for its ability to act as a fungicide, particularly against wood-decay fungi. Due to its reactivity and potential environmental impact, 2,5-dichloro-4-nitrophenol is subject to strict regulations regarding its production, use, and disposal.

2.What is the CAS number for 2,5-dichloro-4-nitrophenol ?

The CAS number of 2,5-dichloro-4-nitrophenol is 5847-57-4.

3.What are another words for 2,5-dichloro-4-nitrophenol ?

Synonyms?for?2,5-dichloro-4-nitrophenol 5847-57-4:2,5-Dichloro-4-nitrophenol;

4.What is 2,5-dichloro-4-nitrophenol (5847-57-4) used for?

Used in Chemical Synthesis:
2,5-Dichloro-4-nitrophenol is utilized as a precursor in the synthesis of dyes and pharmaceuticals, playing a crucial role in the production of these compounds due to its reactive chemical structure.
Used in Pesticide and Fungicide Formulations:
2,5-dichloro-4-nitrophenol serves as an active ingredient in pesticides and fungicides, where it is employed for its biocidal properties to control and prevent the growth of unwanted organisms in agricultural and other settings.
Used in Environmental and Industrial Processes:
While 2,5-dichloro-4-nitrophenol is toxic to aquatic organisms and can lead to long-term environmental damage, it is still used in certain industrial processes. However, its use is tightly regulated due to its classification as a hazardous substance, necessitating careful handling to minimize risks to human health and the environment.

InChI:InChI=1/C6H3Cl2NO3/c7-3-2-6(10)4(8)1-5(3)9(11)12/h1-2,10H

Relevant articles related to 2,5-dichloro-4-nitrophenol:

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Synthesis of macrocyclic urea kinase inhibitors

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, p. 2855 - 2858 (2008/03/13)

The metabolism of 2:4-,2:5-and 3:4-dichloronitrobenzene in the rabbit.

BRAY,JAMES,THORPE

, p. 483 - 490 (2007/10/14)

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