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2,5-Dichloro-4-nitrophenol is a chemical compound characterized by the molecular formula C6H3Cl2NO3. It manifests as a yellow crystalline solid and is recognized for its diverse applications across various industrial sectors.

5847-57-4

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5847-57-4 Usage

Uses

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.

Check Digit Verification of cas no

The CAS Registry Mumber 5847-57-4 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 5,8,4 and 7 respectively; the second part has 2 digits, 5 and 7 respectively.
Calculate Digit Verification of CAS Registry Number 5847-57:
(6*5)+(5*8)+(4*4)+(3*7)+(2*5)+(1*7)=124
124 % 10 = 4
So 5847-57-4 is a valid CAS Registry Number.
InChI:InChI=1/C6H3Cl2NO3/c7-3-2-6(10)4(8)1-5(3)9(11)12/h1-2,10H

5847-57-4Relevant academic research and scientific papers

Synthesis of macrocyclic urea kinase inhibitors

Tao, Zhi-Fu,Sowin, Thomas J.,Lin, Nan-Horng

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

An efficient and convergent route was developed for the synthesis of a novel class of urea-based macrocyclic kinase inhibitors. The synthesis is featured with an efficient urea formation by using a key carbamate intermediate and with a smooth ring-closure olefin metathesis. Furthermore, the hydrogenations of the resulting olefins were investigated in this complex macrocyclic ring system. Georg Thieme Verlag Stuttgart.

Macrocyclic kinase inhibitors

-

Page/Page column 60, (2010/02/14)

Compounds having the formula are useful for inhibiting protein kinases. Also disclosed are methods of making the compounds, compositions containing the compounds, and methods of treatment using the compounds.

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